KAP
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Curette, Nasal
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 874.4420
- Medical specialty
- Ear, Nose, Throat
- Adverse events (MAUDE)
- 2006: 2
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| CURETTE SET, ANTRUM, COAKLEY (K872609) | Military Engineering, Inc. | 1987-07-15 |
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Every clearance here is in the API, with alerts when new ones post.