FDA Device Establishments · JSON-LD · Markdown

LGC Clinical Diagnostics, Inc.

FEI 3003610890 · Manufacture Medical Device · Status: Active

FEI Number3003610890
Owner / OperatorLGC Clinical Diagnostics, Inc. (#9041170)
Address910 Clopper road, Gaithersburg, MD, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)DGQ
Regulation § (21 CFR)866.5700
Proprietary namesACCURUN 52 Multi-Marker Hepatitis Positive Control 2 S3000; MultiChem ID ToRCH Negative Control; ACCURUN 25 ToRCH IgG Positive Control S5000; MultiChem ID TORC IgM Positive Control; ACCURUN 25 Torch IgG Positive Control Series 1000; MultiChem ID TORCH IgG Positive Control; ACCURUN 26 ToRC IgM Positive Control Series 5000; ACCURUN 51 Multi-Marker Hepatitis Positive Control 1 Series 2000; MultiChem ID Rubella IgM Positive Control; AccuPlex rEbola GP/NP Reference Material (0505-0001)

External sources

Source: openFDA. Public-domain (CC0).