CBA — Monitor, Air Embolism, Ultrasonic Class II
FDA product code CBA covers "Monitor, Air Embolism, Ultrasonic", a Class II medical device regulated under 21 CFR 868.2025. Submissions are reviewed by the Anesthesiology panel. At least 1 recent 510(k) clearance has been granted under this product code.
Classification Details
- Product Code
- CBA
- Device Class
- Class II
- Regulation Number
- 868.2025
- Submission Type
- Review Panel
- AN
- Medical Specialty
- Anesthesiology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K780703 | omp laboratories | CUFF PACER | July 17, 1978 |