DeviceClearance

Product code MUI— Radiology

AUTOGEL PAD

Classification name
Media, Coupling, Ultrasound
Device class
Class 2
Regulation
21 CFR 892.1570
Advisory panel
Radiology
Total cleared
34
First cleared
Most recent

Market context for product code MUI

FDA has cleared 34 devices under product code MUI between 1982 and 2026, filed by 26 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

Clearances per year

last 15 years

Top applicants under product code MUI

Recent clearances under product code MUI

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