IQB
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Belt, Wheelchair
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 890.3920
- Medical specialty
- Physical Medicine
- Adverse events (MAUDE)
- 1994: 1 · 1995: 1 · 1996: 1 · 1998: 2 · 1999: 1 · 2002: 3
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.
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| Record | Firm | Date | Builder |
|---|---|---|---|
| WHEELCHAIR BELT (K772421) | Fred Sammons, Inc. | 1978-01-05 | + Add |
| REAR FASTENING SAFETY STRAP (K772420) | Fred Sammons, Inc. | 1978-01-05 | + Add |
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Every clearance here is in the API, with alerts when new ones post.