IWO
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Apron, Protective
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 892.6500
- Medical specialty
- Radiology
- Adverse events (MAUDE)
- 1995: 1 · 1997: 3
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 |
|---|---|---|
| SHIELD, DENTAL X-RAY, PROTECTIVE (K770407) | Worldwide Dental, Inc. | 1977-03-15 |
Track IWO automatically
Every clearance here is in the API, with alerts when new ones post.