DeviceClearance

Product code MGO— General, Plastic Surgery

DEROYAL WOUND DRESSING

Classification name
Closure, Wound, Adhesive
Device class
Class 1
Regulation
21 CFR 878.4018
Advisory panel
General, Plastic Surgery
Total cleared
1
First cleared
Most recent

Market context for product code MGO

FDA has cleared 1 device under product code MGO, all in 1991, filed by 1 applicant company. 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.

Top applicants under product code MGO

Recent clearances under product code MGO

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