IWX
3 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Barrier, Control Panel, X-Ray, Movable
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 892.6500
- Medical specialty
- Radiology
- Adverse events (MAUDE)
- 1996: 1
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 |
|---|---|---|
| A2J MZ 45 LASER LIGHT FOR POSITIONING (K881591) | A2j, Inc. | 1988-04-27 |
| MOBILE LEAD PLASTIC X-RAY BARRIERS (K850813) | Victoreen, Inc. | 1985-04-10 |
| AUTOMATIC FILM PROCESSORIO M. R80 (K781068) | Tecnomed, Inc. | 1978-07-17 |
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Every clearance here is in the API, with alerts when new ones post.