Home › Device types › KGT
Drape, Adhesive, Aerosol
FDA product code KGT · Class 1 · General, Plastic Surgery
4
Registered devices
5
Adverse events
1
Recalls
1
510(k) clearances
Devices with this code
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2008-03-05 | Kapp Surgical Instrument Inc | A portion of the labeled expiration date is missing. The expiration date on approximately half of the pouch labels distributed are missing the last digit of the |
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