GDN
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Knife, Amputation
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 878.4800
- Medical specialty
- General, Plastic Surgery
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| 9-190,9-200,9-210,9-220 AMPUTATION KNIVES, VARIOUS (K851752) | Artiberia | 1985-06-20 |
Track GDN automatically
Every clearance here is in the API, with alerts when new ones post.