KNB
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Instrument, Destructive, Fetal, Obstetric
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 884.4500
- Medical specialty
- Obstetrics/Gynecology
- Flags
- Third-party review eligible
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| CEPHALOTOMY SCISSORS (K890388) | Kinetic Medical Products | 1989-02-13 |
Track KNB automatically
Every clearance here is in the API, with alerts when new ones post.