DeviceClearance

Product code FMA— General Hospital

AROMATIC AND FLAVORED TONGUE DEPRESSOR

Classification name
Depressor, Tongue, Non-Surgical
Device class
Class 1
Regulation
21 CFR 880.6230
Advisory panel
General Hospital
Total cleared
5
First cleared
Most recent

Market context for product code FMA

FDA has cleared 5 devices under product code FMA between 1977 and 1999, filed by 5 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 FMA

Recent clearances under product code FMA

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