FDA 510(k), K173879, MiniMed Mio Advance infusion set

FDA 510(k), K173879, MiniMed Mio Advance infusion set

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510(K) Number: K173879
Device Name: MiniMed Mio Advance infusion set
Manufacturer: Heidi Bjerre Lovkvist
Device Classification Name: Set, Administration, Intravascular
Regulation Number: FPA
Classification Product Code: 12/21/2017
Date Received: 03/05/2018
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital

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