DeviceClearance

Product code GDI— General, Plastic Surgery

DISPOSABLE EXTERNAL CLAMPS

Classification name
Dissector, Surgical, General & Plastic Surgery
Device class
Class 1
Regulation
21 CFR 878.4800
Advisory panel
General, Plastic Surgery
Total cleared
7
First cleared
Most recent

Market context for product code GDI

FDA has cleared 7 devices under product code GDI between 1979 and 1989, filed by 7 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 GDI

Recent clearances under product code GDI

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