DeviceClearance

Product code KQM— General, Plastic Surgery

ADAPTOR: KAPS CINE TO MOELLER BEAMSPLITTER

Classification name
Camera, Surgical And Accessories
Device class
Class 1
Regulation
21 CFR 878.4160
Advisory panel
General, Plastic Surgery
Total cleared
18
First cleared
Most recent

Market context for product code KQM

FDA has cleared 18 devices under product code KQM between 1981 and 1990, filed by 13 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 KQM

Recent clearances under product code KQM

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