Product code NEC— General Hospital

APLICARE SKIN PROTECTANT PREP PAD

Classification name
Bandage, Liquid, Skin Protectant
Device class
Class 1
Regulation
21 CFR 880.5090
Advisory panel
General Hospital
Total cleared
3
First cleared
Most recent

Market context for product code NEC

FDA has cleared 3 devices under product code NEC between 1986 and 1997, filed by 2 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 NEC

Recent clearances under product code NEC

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