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Antisera, Immunoperoxidase, Chlamydia Spp.

FDA product code LKH · Class 1 · Microbiology

1
Registered devices
0
Adverse events
6
Recalls
8
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2006-08-15Encore Medical, LpComplaints received that device used to prepare femur to receive femoral implant would split during surgery.
2006-08-15Encore Medical, LpComplaints received that device used to prepare femur to receive femoral implant would split during surgery.
2006-08-15Encore Medical, LpComplaints received that device used to prepare femur to receive femoral implant would split during surgery.
2006-08-15Encore Medical, LpComplaints received that device used to prepare femur to receive femoral implant would split during surgery.
2006-08-15Encore Medical, LpComplaints received that device used to prepare femur to receive femoral implant would split during surgery.
2006-08-15Encore Medical, LpComplaints received that device used to prepare femur to receive femoral implant would split during surgery.

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