FDA 510(k), K031861, MIX2VIAL TRANSFER DEVICE
FDA 510(k), K031861, MIX2VIAL TRANSFER DEVICE
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$149.00 USD
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510(K) Number: K031861
Device Name: MIX2VIAL 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: 06/16/2003
Decision Date: 07/29/2003
Regulation Medical Specialty: General Hospital
Device Name: MIX2VIAL 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: 06/16/2003
Decision Date: 07/29/2003
Regulation Medical Specialty: General Hospital