Medicaid Provider Spending

$1.09 trillion in Medicaid claims data, 2018–2024 · 617K+ providers

PRIME DIAGNOSTICS LAB INC.

NPI: 1093351470 · SOUTHFIELD, MI 48034 · Clinical Medical Laboratory · NPI assigned 11/20/2019

$143K
Total Medicaid Paid
3,419
Total Claims
2,057
Beneficiaries
8
Codes Billed
2024-07
First Month
2024-12
Last Month

Provider Details

Authorized OfficialHINA SHAKIL, SYEDA (CEO)
NPI Enumeration Date11/20/2019

Monthly Spending Trend

Yearly Breakdown

YearClaimsTotal Paid
2024 3,419 $143K

Billing Codes

CodeDescriptionClaimsBeneficiariesTotal Paid
87502 Infectious agent detection by nucleic acid, influenza virus, for multiple types or subtypes, includes all targets 604 399 $38K
G0481 Drug test(s), definitive, utilizing (1) drug identification methods able to identify individual drugs and distinguish between structural isomers (but not necessarily stereoisomers), including, but not limited to gc/ms (any type, single or tandem) and lc/ms (any type, single or tandem and excluding immunoassays (e.g., ia, eia, elisa, emit, fpia) and enzymatic methods (e.g., alcohol dehydrogenase)), (2) stable isotope or other universally recognized internal standards in all samples (e.g., to control for matrix effects, interferences and variations in signal strength), and (3) method or drug-specific calibration and matrix-matched quality control material (e.g., to control for instrument variations and mass spectral drift); qualitative or quantitative, all sources, includes specimen validity testing, per day; 8-14 drug class(es), including metabolite(s) if performed 324 304 $34K
87636 Infectious agent detection by nucleic acid; SARS-CoV-2 and influenza virus types A and B 252 141 $29K
80307 Drug test(s), presumptive, any number of drug classes; immunoassay 292 276 $12K
87426 Infectious agent antigen detection, SARS-CoV-2 (COVID-19) 602 399 $12K
87400 1,199 399 $11K
87637 Infectious agent detection by nucleic acid; SARS-CoV-2, influenza, and RSV 45 38 $5K
G0480 Drug test(s), definitive, utilizing (1) drug identification methods able to identify individual drugs and distinguish between structural isomers (but not necessarily stereoisomers), including, but not limited to gc/ms (any type, single or tandem) and lc/ms (any type, single or tandem and excluding immunoassays (e.g., ia, eia, elisa, emit, fpia) and enzymatic methods (e.g., alcohol dehydrogenase)), (2) stable isotope or other universally recognized internal standards in all samples (e.g., to control for matrix effects, interferences and variations in signal strength), and (3) method or drug-specific calibration and matrix-matched quality control material (e.g., to control for instrument variations and mass spectral drift); qualitative or quantitative, all sources, includes specimen validity testing, per day; 1-7 drug class(es), including metabolite(s) if performed 101 101 $284.25