DeviceClearance

Product code CBP— Anesthesiology

CPR MICROMASK

Classification name
Valve, Non-Rebreathing
Device class
Class 2
Regulation
21 CFR 868.5870
Advisory panel
Anesthesiology
Total cleared
103
First cleared
Most recent

Market context for product code CBP

FDA has cleared 103 devices under product code CBP between 1977 and 2024, filed by 67 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

last 15 years

Top applicants under product code CBP

Recent clearances under product code CBP

1–100 of 103

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