DeviceClearance

Product code GDJ— General, Plastic Surgery

VESSEL OCCLUDER

Classification name
Clamp, Surgical, General & Plastic Surgery
Device class
Class 1
Regulation
21 CFR 878.4800
Advisory panel
General, Plastic Surgery
Total cleared
32
First cleared
Most recent

Market context for product code GDJ

FDA has cleared 32 devices under product code GDJ between 1976 and 2016, 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 GDJ

Recent clearances under product code GDJ

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