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Igg (Fd Fragment Specific), Antigen, Antiserum, Control

FDA product code DAQ · Class 1 · Immunology

0
Registered devices
1
Adverse events
1
Recalls
1
510(k) clearances

Recent recalls

DateFirmReason
2018-12-17Roche Diagnostics CorporationNew endogenous interference claims have been established for the following assays used on the cobas c 311 analyzer and the cobas c 501, 502, 701, 702, and Modul

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.