FDA 510(k), K162304, Q2 Multiport IV Administration Sets and Extension Sets, Checkmate Multiport IV Administration Sets, Q2 Extension Sets

FDA 510(k), K162304, Q2 Multiport IV Administration Sets and Extension Sets, Checkmate Multiport IV Administration Sets, Q2 Extension Sets

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510(K) Number: K162304
Device Name: Q2 Multiport IV Administration Sets and Extension Sets, Checkmate Multiport IV Administration Sets, Q2 Extension Sets
Manufacturer: QUEST MEDICAL, INC.
Device Classification Name: set, administration, intravascular
Regulation Number: 880.5440
Classification Product Code: FPA
Date Received: 08/17/2016
Decision Date: 12/06/2016
Regulation Medical Specialty: General Hospital

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