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FDA 510(k) Application Details - K980859
Device Classification Name
Dialyzer, High Permeability With Or Without Sealed Dialysate System
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510(K) Number
K980859
Device Name
Dialyzer, High Permeability With Or Without Sealed Dialysate System
Applicant
MINNTECH CORP.
14605 28TH AVE. NORTH
MINNEAPOLIS, MN 55447 US
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Contact
MARK MURPHY
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Regulation Number
876.5860
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Classification Product Code
KDI
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More FDA Info for this Product Code
Date Received
03/05/1998
Decision Date
05/12/1998
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
GU - Gastroenterology & Urology
Review Advisory Committee
GU - Gastroenterology & Urology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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