• FDA DYMISTA NDA 202236 approval records — 22 FDA documents, 848 pages
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FDA 510(k) K031861, MIX2VIAL TRANSFER DEVICE, by Medimop Medical Projects, Ltd.

FDA 510(k) K031861, MIX2VIAL TRANSFER DEVICE, by Medimop Medical Projects, Ltd.

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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
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