CHROM MEDICAL LABS NPI 1427657360

NPI Details

CHROM MEDICAL LABS is a clinical medical laboratory in Jenks, OK. The provider is (1) A clinical laboratory is a facility for the biological, microbiological, serological, chemical, immunohematological, hematological, biophysical, cytological, pathological, or other examination of materials derived from the human body for the purpose of providing information for the diagnosis, prevention, or treatment of any disease or impairment of, human beings. These examinations also include procedures to determine, measure, or otherwise describe the presence or absence of various substances or organisms in the body. Facilities only collecting or preparing specimens (or both) or only serving as a mailing service and not performing testing are not considered clinical laboratories. (2) Any facility that examines materials from the human body for purposes of providing information for the diagnosis, prevention, or treatment of any disease or impairment of, or the assessment of, the health of human beings. Typical divisions of a clinical laboratory include hematology, cytology, bacteriology, histology, biochemistry, medical toxicology, and serology. CHROM MEDICAL LABS NPI is 1427657360. The provider is registered as an organization entity type.
The provider Is Doing Business As Chrom Medical Labs.

The provider's business location address is:

201 W MAIN ST STE 101A
JENKS, OK
ZIP 74037-939
Phone: (561) 849-0635

The provider's authorized official is Graig Robinson .
The authorized official title is Chairman and has the following contact phone number (954) 790-1104.

The following top HCPCS codes were publicly reported for this provider under the Medicare program for the year 2016. The reported codes are based on the top codes for each available Medicare specialty, excluding evaluation and management codes.

• Provision of covid-19 test, nonprescription self-administered and self-collected use, fda approved, authorized or cleared, one test count (HCPCS:K1034)
• Molecular pathology procedure level 1 (HCPCS:81400)
• Gene analysis (cystic fibrosis transmembrane conductance regular) full gene sequence (HCPCS:81223)
• Gene analysis (partner and localizer of brca2) full sequence analysis (HCPCS:81307)
• Gene analysis (muts homolog 6 [e coli]) full sequence analysis (HCPCS:81298)
• Gene analysis (postmeiotic segregation increased 2 [s cerevisiae]) full sequence analysis (HCPCS:81317)
• Gene analysis (mpl proto-oncogene, thrombopoietin receptor) sequence analysis of exon 10 (HCPCS:81339)
• Gene analysis (glucose-6-phosphate dehydrogenase) full sequence analysis (HCPCS:81249)
• Gene analysis (glucose-6-phosphatase, catalytic subunit) common variants (HCPCS:81250)
• Gene analysis (bloom syndrome, recq helicase-like) (HCPCS:81209)
• Gene analysis (fanconi anemia, complementation group c) common variant (HCPCS:81242)
• Gene analysis (coagulation factor ix) full sequence analysis (HCPCS:81238)
• Genomic sequence analysis panel for severe inherited conditions with sequencing of 15 or more genes (HCPCS:81443)
• Gene analysis panel for hereditary disorders of the peripheral nervous system (HCPCS:81448)
• Gene analysis (5, 10-methylenetetrahydrofolate reductase) common variants (HCPCS:81291)
• Gene analysis (methyl cpg binding protein 2) full sequence analysis (HCPCS:81302)
• Gene analysis (huntingtin) for abnormal alleles (HCPCS:81271)
• Gene analysis (partner and localizer of brca2) targeted sequence analysis (HCPCS:81309)
• Gene analysis (poly[a] binding protein nuclear 1) for abnormal alleles (HCPCS:81312)
• Gene analysis (fragile x mental retardation) abnormal alleles (HCPCS:81243)
• Gene analysis (fragile x mental retardation 2) for abnormal alleles (HCPCS:81171)
• Gene analysis (cystatin b) of full sequence (HCPCS:81189)
• Gene analysis (neurotrophic receptor tyrosine kinase 1) translocation analysis (HCPCS:81191)
• Gene analysis (neurotrophic receptor tyrosine kinase 2) translocation analysis (HCPCS:81192)
• Gene analysis (aspartoacylase) (HCPCS:81200)
• Gene analysis (glucosidase, beta, acid) common variants (HCPCS:81251)
• Gene analysis (hexosaminidase a) common variants (HCPCS:81255)
• Gene analysis (survival of motor neuron 1, telomeric) for dosage/deletion (HCPCS:81329)
• Gene analysis (inhibitor of kappa light polypeptide gene enhancer in b-cells, kinase complex-associated protein) common variants (HCPCS:81260)
• Gene analysis (peripheral myelin protein 22), full sequence analysis (HCPCS:81325)
• Gene analysis (calcium voltage-gated channel subunit alpha1 a) of full sequence (HCPCS:81185)
• Gene analysis (frataxin) of full sequence (HCPCS:81286)
• Gene analysis (hemochromatosis) common variants (HCPCS:81256)
• Gene analysis (cytochrome p450, family 2, subfamily d, polypeptide 6) common variants (HCPCS:81226)
• Gene analysis (cytochrome p450, family 2, subfamily c, polypeptide 19) common variants (HCPCS:81225)
• Gene analysis (adenomatous polyposis coli), full gene sequence (HCPCS:81201)
• Gene analysis (muts homolog 2, colon cancer, nonpolyposis type 1) full sequence analysis (HCPCS:81295)

The enumeration date for this NPI number is 10/21/2020 and was last updated on 5/30/2023.

Taxonomy Codes

The NPI record includes the healthcare provider taxonomy classification, state license number and state of licensure. The following information regarding the scope of practice of this provider is available: