FRZ
5 FDA 510(k) clearances · Product code
125 daysmedian time to decision
468 days90th percentile
5clearances measured
FDA profile
- Official device name
- Device, Patient Transfer, Powered
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 880.6775
- Medical specialty
- General Hospital
- Adverse events (MAUDE)
- 1995: 1 · 1998: 2 · 2012: 5
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 |
|---|---|---|
| ZEPHYR 'X-SERIES PATIENT TRANSFER SLED (K121929) | Diacor, Inc. | 2013-01-17 |
| INVALIFT (K910830) | American Invalift Corp. | 1992-06-09 |
| LCI MEDICAL INC AIR/PAL (K841728) | Lehigh Consolidated Industries | 1984-06-05 |
| CELLTRAK-B (K834585) | R&D Systems, Inc. | 1984-05-02 |
| TENDER LIFTING CARE (K840796) | Lancer Assoc. | 1984-04-20 |
Track FRZ automatically
Every clearance here is in the API, with alerts when new ones post.