DeviceClearance

Product code KMJ— General Hospital

LUBRICATING JELLY

Classification name
Lubricant, Patient
Device class
Class 1
Regulation
21 CFR 880.6375
Advisory panel
General Hospital
Total cleared
49
First cleared
Most recent

Market context for product code KMJ

FDA has cleared 49 devices under product code KMJ between 1977 and 2015, filed by 42 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 KMJ

Recent clearances under product code KMJ

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