FZH
4 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Apparatus, Air Handling, Room
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 878.5070
- Medical specialty
- General, Plastic Surgery
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| CARDIO-PAK LAPAROTOMY PACK (K923233) | Cardio-Med-Associates, Inc. | 1993-03-20 |
| MODEL UCA / SPEC SYSTEM UCA (K875305) | Spec Systems, Inc. | 1988-01-27 |
| ULTRAFLOW (K871901) | Custom Industries, Inc. | 1987-06-01 |
| OPERATING ROOM VENTILATOR (K770084) | Dupaco, Inc. | 1977-02-23 |
Track FZH automatically
Every clearance here is in the API, with alerts when new ones post.