FDA product code QJG
Device System, Imaging, Tympanic Membrane And Middle Ear
Radiology·Class 2·21 CFR 892.1560
US regulatory classifications
- US Product Code (FDA)
- QJGView Product Code Classification →
- US Risk Class (FDA)
- Class 2
- US Regulation (CFR)
- 21 CFR 892.1560View 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.