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
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
- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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