DeviceClearance

Product code FQL— General Hospital

ELASTIC COMPRESSION ANKLET

Classification name
Stocking, Medical Support (For General Medical Purposes)
Device class
Class 1
Regulation
21 CFR 880.5780
Advisory panel
General Hospital
Total cleared
6
First cleared
Most recent

Market context for product code FQL

FDA has cleared 6 devices under product code FQL between 1982 and 1994, 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 FQL

Adverse events under product code FQL

product code FQL
Other
1
Total
1

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recent clearances under product code FQL

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