DeviceClearance

Product code FLG— General Hospital

ALSA-KLENZ

Classification name
Cleaner, Ultrasonic, Medical Instrument
Device class
Class 1
Regulation
21 CFR 880.6150
Advisory panel
General Hospital
Total cleared
19
First cleared
Most recent

Market context for product code FLG

FDA has cleared 19 devices under product code FLG between 1977 and 1994, filed by 12 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 FLG

Recent clearances under product code FLG

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