Product code GDC— General, Plastic Surgery

AMSCO ENDOSCOPY TABLE

Classification name
Table, Operating-Room, Electrical
Device class
Class 1
Regulation
21 CFR 878.4960
Advisory panel
General, Plastic Surgery
Total cleared
18
First cleared
Most recent

Market context for product code GDC

FDA has cleared 18 devices under product code GDC between 1982 and 1997, filed by 12 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 GDC

Adverse events under product code GDC

product code GDC
Malfunction
791
Total
791

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recent clearances under product code GDC

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