FDA 510(k), K160252, OmniPod Insulin Management System
FDA 510(k), K160252, OmniPod Insulin Management System
Device Name: OmniPod Insulin Management System
Manufacturer: MATTHEW KING
Device Classification Name: Pump, Infusion, Insulin
Regulation Number: LZG
Classification Product Code: KXA
Date Received: 02/01/2016
Decision Date: 04/27/2016
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
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