FDA 510(k) K200529, Orion, lnteracoustics A/S

FDA 510(k) K200529, Orion, lnteracoustics A/S

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510(K) Number: K200529
Device Name: Orion
Manufacturer: lnteracoustics A/S
Device Classification Name: Apparatus, Vestibular Analysis
Regulation Number:
Classification Product Code: LXV
Date Received: 03/02/2020
Decision Date: 08/12/2020
Regulation Medical Specialty: Ear Nose & Throat
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