FNK
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Bed, Hydraulic, Adjustable Hospital
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 880.5110
- Medical specialty
- General Hospital
- Adverse events (MAUDE)
- 1992: 18 · 1993: 11 · 1994: 2 · 1995: 1 · 1996: 1 · 2015: 17
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 |
|---|---|---|
| OPTIMA DELIVERY BED (MODELS 33901, 33903, 33902, 33905) (K944929) | Merivaara Instrumentarium Corp. | 1994-11-22 |
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Every clearance here is in the API, with alerts when new ones post.