Product code CBC— General Hospital
AMBU SUCTION BOOSTER
- Classification name
- Bottle, Collection And Trap, Breathing System (Uncalibrated)
- Device class
- Class 2
- Regulation
- 21 CFR 880.6740
- Advisory panel
- General Hospital
- Total cleared
- 3
- First cleared
- Most recent
Market context for product code CBC
FDA has cleared devices under product code CBC between 1976 and 1993, filed by 3 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.
Clearances per year
- 1993
- 1979
- 1976
Top applicants under product code CBC
Recent clearances under product code CBC
Data sourced from openFDA. This site is unofficial and independent of the FDA.