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FDA 510(k) Application Details - K954906
Device Classification Name
Introducer, Catheter
More FDA Info for this Device
510(K) Number
K954906
Device Name
Introducer, Catheter
Applicant
BECTON DICKINSON VASCULAR ACCESS, INC.
9450 SOUTH STATE ST.
SANDY, UT 84070 US
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Contact
C J WELLE
Other 510(k) Applications for this Contact
Regulation Number
870.1340
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Classification Product Code
DYB
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More FDA Info for this Product Code
Date Received
10/25/1995
Decision Date
04/08/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
CV - Cardiovascular
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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