FWL
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Camera, Cine, Endoscopic, Without Audio
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 878.4160
- Medical specialty
- General, Plastic Surgery
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| WECO ENDOSCOPIC SYSTEM WITH FIBER OPTIC LIGHT (K951519) | Wells Johnson Co. | 1995-06-14 |
| STORZ MODEL 62 ENT CAMERA SYSTEM (K883760) | Storz Instrument Co. | 1988-09-28 |
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Every clearance here is in the API, with alerts when new ones post.