FDA Device Establishments · JSON-LD · Markdown

CLINICAL REFERENCE LABORATORY, INC.

FEI 1910144 · Complaint File Establishment per 21 CFR 820.198 Repack or Relabel Medical Device · Status: Active

FEI Number1910144
Owner / OperatorClinical Reference Laboratory (#10038059)
Address8433 Quivira Rd, Lenexa, KS, US
Registration expiry2026
Initial importer flagN
Registered products11
Product codes (top 20)NFV, NFW, NFY, LCM, NFT, NGG, PTH, NGL, PTG, QAW, QBF
Regulation § (21 CFR)862.3170, 862.3870, 862.3250, 862.3100, 862.3610, 862.3150, 862.3650, 862.3620, 862.3910, 862.3700
Proprietary namesCRL Stat

External sources

Source: openFDA. Public-domain (CC0).