CBA
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Monitor, Air Embolism, Ultrasonic
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 868.2025
- Medical specialty
- Anesthesiology
- Flags
- Third-party review eligible
- Adverse events (MAUDE)
- 1993: 1
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| CUFF PACER (K780703) | Omp Laboratories, Inc. | 1978-07-17 |
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