KFX
4 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Assembly, Thigh/Knee/Shank/Ankle/Foot, External
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 890.3500
- Medical specialty
- Physical Medicine
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| STERILE LEMAITRE GLOW 'N TELL TAPE (K932184) | Vascutech, Inc. | 1993-07-22 |
| IPOS G.L.P. SYSTEM (K833868) | Ipos Luneburg | 1983-11-28 |
| REGNELL HYDRAULIC FEMORAL PROTHESIS (K830285) | Besco Financial Service | 1983-03-09 |
| ETHYLENE OXIDE STERILIZ. PARAMETRIC REL. (K822240) | American Mcgaw | 1982-12-30 |
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Every clearance here is in the API, with alerts when new ones post.