Product code KMF— General Hospital

DERMAGRAN HYDROPHILIC OINTMENT

Classification name
Bandage, Liquid
Device class
Class 1
Regulation
21 CFR 880.5090
Advisory panel
General Hospital
Total cleared
222
First cleared
Most recent

Market context for product code KMF

FDA has cleared 222 devices under product code KMF between 1977 and 2024, filed by 114 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

last 15 years

Top applicants under product code KMF

Recent clearances under product code KMF

1–100 of 222

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