CBD
3 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Bottle, Collection, Breathing System (Calibrated)
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 880.6740
- Medical specialty
- General Hospital
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| IMV SYSTEM (K780340) | Lkb Instruments, Inc. | 1978-11-27 |
| VALVE, PRESSURE, DEMAND (K770665) | Mcgaw Respiratory Therapy | 1977-04-15 |
| VACON TM (K770369) | Diemolding Corp. | 1977-03-01 |
Track CBD automatically
Every clearance here is in the API, with alerts when new ones post.