KBD
3 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Scissors, Nasal
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 874.4420
- Medical specialty
- Ear, Nose, Throat
- Adverse events (MAUDE)
- 1996: 2 · 1997: 3
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 |
|---|---|---|
| 13-320,13-330 TWO TYPES NAZAL SCISSORS-HEYMAN,BECK (K851763) | Artiberia | 1985-06-11 |
| EAR SPOON (K822524) | Kelleher Corp. | 1982-09-09 |
| SURGICAL SCISSORS (K791124) | Xomed, Inc. | 1979-06-27 |
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Every clearance here is in the API, with alerts when new ones post.