Product code FWX— General, Plastic Surgery

ALM OPERATING TABLES

Classification name
Table, Operating-Room, Mechanical
Device class
Class 1
Regulation
21 CFR 878.4950
Advisory panel
General, Plastic Surgery
Total cleared
3
First cleared
Most recent

Market context for product code FWX

FDA has cleared 3 devices under product code FWX between 1982 and 1988, filed by 3 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 FWX

Recent clearances under product code FWX

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