FDA Product Code
FDA Product Code KFX — Clearance Directory
- Device Class
- Class II
- Assigned Panel
- Physical Medicine
- 21 CFR Citation
- 890.3500
510(k) Clearances — 4 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K932184 | STERILE LEMAITRE GLOW 'N TELL TAPE | Vascutech, Inc. | 1993-07-22 | Traditional | PDF ↗ |
| K833868 | IPOS G.L.P. SYSTEM | Ipos Luneburg | 1983-11-28 | Traditional | PDF ↗ |
| K830285 | REGNELL HYDRAULIC FEMORAL PROTHESIS | Besco Financial Service | 1983-03-09 | Traditional | PDF ↗ |
| K822240 | ETHYLENE OXIDE STERILIZ. PARAMETRIC REL. | American Mcgaw | 1982-12-30 | Traditional | PDF ↗ |
Product code KFX · Class II · Physical Medicine. Data: openFDA.