FZK
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Chair, Surgical, Non-Electrical
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 878.4950
- Medical specialty
- General, Plastic Surgery
- Adverse events (MAUDE)
- 1997: 1 · 1999: 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 |
|---|---|---|
| OLYMPUS MOBILE CHAIR/COUCH (K962528) | Keymed (Medical & Industrial Equipment), Ltd. | 1996-12-12 |
| NEUTRAL POS-CHAIR SURGEON CHAIR (K842030) | Neutral Pos-Chair Co. | 1984-07-23 |
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Every clearance here is in the API, with alerts when new ones post.