FDA Device Establishments · JSON-LD · Markdown

ACCUMETRA

FEI 3014498605 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active

FEI Number3014498605
Owner / OperatorAccumetra (#10057556)
AddressAccumetra, 7 Corporate Drive, Clifton Park, NY, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)LHO
Regulation § (21 CFR)892.1940
Proprietary namesCTLX1

External sources

Source: openFDA. Public-domain (CC0).