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Device System, Imaging, Tympanic Membrane And Middle Ear

FDA product code QJG · 2 cleared devices

Class 2 Radiology
Regulation
21 CFR 892.1560
Review panel
EN
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
2019-12-05 – 2022-09-26

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

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