DeviceClearance

Product code KDC— General, Plastic Surgery

ALTRACLUDE

Classification name
Instrument, Surgical, Disposable
Device class
Class 1
Regulation
21 CFR 878.4800
Advisory panel
General, Plastic Surgery
Total cleared
67
First cleared
Most recent

Market context for product code KDC

FDA has cleared 67 devices under product code KDC between 1976 and 1994, filed by 46 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 KDC

Recent clearances under product code KDC

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