Product code KCW— General, Plastic Surgery

APILUS ELECTROPIL

Classification name
Epilator, High Frequency, Needle-Type
Device class
Class 1
Regulation
21 CFR 878.5350
Advisory panel
General, Plastic Surgery
Total cleared
43
First cleared
Most recent

Market context for product code KCW

FDA has cleared 43 devices under product code KCW between 1978 and 1996, filed by 25 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

last 15 years

Top applicants under product code KCW

Recent clearances under product code KCW

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