FTI
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Lamp, Endoscope, Incandescent
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 876.1500
- Medical specialty
- Gastroenterology, Urology
- Flags
- Third-party review eligible
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| CLARUS MODEL 5197 SIGHTLITE (K971455) | Clarus Medical Systems, Inc. | 1997-05-20 |
| OXFORD OPTRONIX MPM 3S (K914397) | Dia-Stron, Ltd. | 1992-11-16 |
Track FTI automatically
Every clearance here is in the API, with alerts when new ones post.