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FDA 510(k) K160783, Procellera, by Vomaris Innovations, Inc.

FDA 510(k) K160783, Procellera, by Vomaris Innovations, Inc.

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510(K) Number: K160783
Device Name: Procellera
Manufacturer: Vomaris Innovations, Inc.
Device Classification Name: dressing, wound, drug
Regulation Number:
Classification Product Code: FRO
Date Received: 03/22/2016
Decision Date: 09/07/2016
Regulation Medical Specialty:
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