DeviceClearance

Product code MAW— General, Plastic Surgery

KEY VASCULAR BOOTIES

Classification name
Marker, Suture Identification
Device class
Class 1
Regulation
21 CFR 878.4800
Advisory panel
General, Plastic Surgery
Total cleared
1
First cleared
Most recent

Market context for product code MAW

FDA has cleared 1 device under product code MAW, all in 1989, 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 MAW

Recent clearances under product code MAW

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