FPS
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Board, Bed
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 880.6070
- Medical specialty
- General Hospital
- Flags
- GMP exempt
- Adverse events (MAUDE)
- 1997: 1 · 2003: 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 |
|---|---|---|
| BED BOARD (K780230) | Biomet, Inc. | 1978-02-28 |
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Every clearance here is in the API, with alerts when new ones post.