FTT
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Camera, Still, Surgical
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 878.4160
- Medical specialty
- General, Plastic Surgery
- Adverse events (MAUDE)
- 2007: 2 · 2017: 13
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| STEREOMED CAMERA (K823534) | Diseases of the Skin Clinic, P.A. | 1982-12-15 |
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Every clearance here is in the API, with alerts when new ones post.