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FDA product code QJG

Device System, Imaging, Tympanic Membrane And Middle Ear

RadiologyClass 221 CFR 892.1560
Verified
US regulatory classifications
US Product Code (FDA)
QJG
View Product Code Classification
US Risk Class (FDA)
Class 2
US Regulation (CFR)
21 CFR 892.1560
View CFR Regulation
Medical specialty
Radiology
Device characteristics
GMP exempt
No
Implantable
No
Life-sustaining
No
Third party review
Not Eligible
Definition

Is intended for use as an imaging tool for visualization of the human tympanic membrane and middle ear space.

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About this record

Device System, Imaging, Tympanic Membrane And Middle Ear is a medical device type in the Radiology specialty. This page includes real-world medical device registration data worldwide for this device type, with registrations from US FDA, Brazil ANVISA, and other global markets.

View regulatory classifications, recent 510(k) clearances, active device registrations, and similar products registered globally under this device category. Pure Global AI's free directory provides comprehensive worldwide registration intelligence across 7,000+ medical device types and 21 specialties.