FDA 510(k), K062482, VENTED VIAL ADAPTER TRANSFER DEVICE

FDA 510(k), K062482, VENTED VIAL ADAPTER TRANSFER DEVICE

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510(K) Number: K062482
Device Name: VENTED VIAL ADAPTER TRANSFER DEVICE
Manufacturer: MEDIMOP MEDICAL PROJECTS, LTD.
Device Classification Name: Set, I.V. Fluid Transfer
Regulation Number: 880.5440
Classification Product Code: LHI
Date Received: 08/24/2006
Decision Date: 11/03/2006
Regulation Medical Specialty: General Hospital

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