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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
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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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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