DeviceClearance

Product code EMF— General, Plastic Surgery

27-210 PLASTER KNIFE (REINER)

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

Market context for product code EMF

FDA has cleared 21 devices under product code EMF between 1978 and 2008, filed by 16 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 EMF

Recent clearances under product code EMF

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