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Indirect Fluorescent Antibody Test, Entamoeba Histolytica & Rel Sp

FDA product code GWD · Class 2 · Microbiology

2
Registered devices
0
Adverse events
3
Recalls
2
510(k) clearances

Devices with this code

E.histolytica Antibody 96Tests — SCIMEDX CORPORATIONE.histolytica Antibody 96 Test with Calibrator — SCIMEDX CORPORATION

Recent recalls

DateFirmReason
2007-07-16Davol, Inc., Sub. C. R. Bard, Inc.Malformed constructs (straight shots) may form causing injury to user/patient
2003-11-20Power Medical Interventionsimproper staple formation or anvil jam
2003-11-20Power Medical Interventionsimproper staple formation or anvil jam

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