Product code CBD— General Hospital

IMV SYSTEM

Classification name
Bottle, Collection, Breathing System (Calibrated)
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 CBD

FDA has cleared 3 devices under product code CBD between 1977 and 1978, 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 CBD

Recent clearances under product code CBD

Data sourced from openFDA. This site is unofficial and independent of the FDA.