KDM
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Sigmoidoscope, Rigid, Non-Electrical
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 876.1500
- Medical specialty
- Gastroenterology, Urology
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| SAPIMED DISPOSABLE SIGMOIDOSCOPE (K070915) | Sapimed S.P.A. | 2007-07-06 |
Track KDM automatically
Every clearance here is in the API, with alerts when new ones post.