DeviceClearance

Product code FMC— General Hospital

AMPCO SKIN SCRUB TRAY

Classification name
Patient Examination Glove
Device class
Class 1
Regulation
21 CFR 880.6250
Advisory panel
General Hospital
Total cleared
34
First cleared
Most recent

Market context for product code FMC

FDA has cleared 34 devices under product code FMC between 1977 and 2004, filed by 30 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 FMC

Recent clearances under product code FMC

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