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FDA 510(k), K122265, VIALOK SINGLE VIAL ACCESS DEVICE VENTED
FDA 510(k), K122265, VIALOK SINGLE VIAL ACCESS DEVICE VENTED
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510(K) Number: K122265
Device Name: VIALOK SINGLE VIAL ACCESS DEVICE VENTED
Manufacturer: YUKON MEDICAL, LLC
Device Classification Name: Set, I.V. Fluid Transfer
Regulation Number: 880.5440
Classification Product Code: LHI
Date Received: 07/30/2012
Decision Date: 08/14/2012
Regulation Medical Specialty: General Hospital
Device Name: VIALOK SINGLE VIAL ACCESS DEVICE VENTED
Manufacturer: YUKON MEDICAL, LLC
Device Classification Name: Set, I.V. Fluid Transfer
Regulation Number: 880.5440
Classification Product Code: LHI
Date Received: 07/30/2012
Decision Date: 08/14/2012
Regulation Medical Specialty: General Hospital
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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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