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 3 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

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.