FDA 510(k), K211868, MYAH

FDA 510(k), K211868, MYAH

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510(K) Number: K211868
Device Name: MYAH
Manufacturer: Alessia Magnanini
Device Classification Name: Device, Analysis, Anterior Segment
Regulation Number: MXK
Classification Product Code: 06/16/2021
Date Received: 03/01/2022
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Ophthalmic

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