KJF
4 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- System, Suspension, Cell Culture
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 864.2240
- Medical specialty
- Hematology
- Flags
- GMP exempt
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| LIFECELL RECOVERY CONTAINER (K893787) | Baxter Healthcare Corp | 1989-06-23 |
| AMICON VITAFIBER FLO-PATH BIORECT/VLS CELL CULT SY (K892645) | Amicon, Inc. | 1989-06-13 |
| TOOTH PRESERVING SYSTEM (K875221) | Biological Rescue Products, Inc. | 1988-04-14 |
| CELL (K780305) | Dynatech Laboratories, Inc. | 1978-03-27 |
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Every clearance here is in the API, with alerts when new ones post.