FDA 510(k) Application Details - K111577

Device Classification Name Set, I.V. Fluid Transfer

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510(K) Number K111577
Device Name Set, I.V. Fluid Transfer
Applicant MEDLINE INDUSTRIES, INC.
ONE MEDLINE PLACE
MUNDELEIN, IL 60060 US
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Contact MATT CLAUSEN
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Regulation Number 880.5440

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Classification Product Code LHI
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Date Received 06/07/2011
Decision Date 09/08/2011
Decision SESE - SUBST EQUIV
Classification Advisory Committee HO - General Hospital
Review Advisory Committee HO - General Hospital
Statement / Summary / Purged Status Statement
Type Traditional
Reviewed By Third Party N
Expedited Review



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