FDA Device Establishments · JSON-LD · Markdown

BIOCHECK, INC.

FEI 3002564473 · Manufacture Device in the United States for Export Only · Status: Active

FEI Number3002564473
Owner / OperatorBIOCHECK, INC. (#9033543)
Address3451 Vincent Rd, Pleasant Hill, CA, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)QAT
Regulation § (21 CFR)866.5830
Proprietary namesDxDATA Protein Gene Product 9.5 (PGP 9.5) CLIA Kit, DXDA-1004; DxDATA Glial Fibrillary Acidic Protein (GFAP) CLIA Kit, DXDA-1003

External sources

Source: openFDA. Public-domain (CC0).