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Lactoferrin ELISA

Immundiagnostik AG · Model K 6870.US · UDI-DI 04050598010406

DEG
8
510(k) clearances
0
Adverse events
1
Recalls
10
Facilities

Recalls

DateFirmReason
2023-03-27IMMUNDIAGNOSTIK, IncMarketed without a 510k

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.