FQL
6 FDA 510(k) clearances · Product code
54 daysmedian time to decision
117 days90th percentile
6clearances measured
FDA profile
- Official device name
- Stocking, Medical Support (For General Medical Purposes)
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 880.5780
- Medical specialty
- General Hospital
- Flags
- GMP exempt
- Adverse events (MAUDE)
- 1992: 2 · 1995: 2
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 |
|---|---|---|
| SOFT SOCK (K944240) | Silipos, Inc. | 1994-12-27 |
| ELASTIC COMPRESSION ANKLET (K823789) | Orthopaedic Resources Corp. | 1983-01-07 |
| ELASTIC COMPRESSION ANKLET (K823350) | Podiatry Products Corp. | 1982-12-03 |
| VITASAN (K821259) | Selomas, Inc. | 1982-06-23 |
| VITOFIT (K821260) | Selomas, Inc. | 1982-06-23 |
| VENES CUSTON RX (K820484) | Jung Products, Inc. | 1982-03-18 |
Track FQL automatically
Every clearance here is in the API, with alerts when new ones post.