FDA 510(k), K111577, MEDLINE VIAL DECANTER

FDA 510(k), K111577, MEDLINE VIAL DECANTER

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510(K) Number: K111577
Device Name: MEDLINE VIAL DECANTER
Manufacturer: MATT CLAUSEN
Device Classification Name: Set, I.V. Fluid Transfer
Regulation Number: LHI
Classification Product Code: KXA
Date Received: 06/07/2011
Decision Date: 09/08/2011
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
  • 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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