Product code FQA— General Hospital

COUNTWAY SYS. SOILED SPONGES-BLOOD LOS

Classification name
Scale, Surgical Sponge
Device class
Class 1
Regulation
21 CFR 880.2740
Advisory panel
General Hospital
Total cleared
1
First cleared
Most recent

Market context for product code FQA

FDA has cleared 1 device under product code FQA, all in 1983, filed by 1 applicant company. 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.

Top applicants under product code FQA

Recent clearances under product code FQA

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