Product code GEO— General, Plastic Surgery

GENERAL SURGICAL FILES

Classification name
File, Surgical, General & Plastic Surgery
Device class
Class 1
Regulation
21 CFR 878.4800
Advisory panel
General, Plastic Surgery
Total cleared
2
First cleared
Most recent

Market context for product code GEO

FDA has cleared 2 devices under product code GEO between 1983 and 1984, filed by 2 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 GEO

Recent clearances under product code GEO

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