DeviceClearance

Product code BWB— Anesthesiology

CAT. 9 ANESTHESIOLOGY RESPIRATORY DEV

Classification name
Forceps, Tube Introduction
Device class
Class 1
Regulation
21 CFR 868.5780
Advisory panel
Anesthesiology
Total cleared
6
First cleared
Most recent

Market context for product code BWB

FDA has cleared 6 devices under product code BWB between 1982 and 1988, filed by 3 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

Clearances per year

Top applicants under product code BWB

Recent clearances under product code BWB

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