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FDA 510(k) Application Details - K954953
Device Classification Name
Anesthesia Conduction Kit
More FDA Info for this Device
510(K) Number
K954953
Device Name
Anesthesia Conduction Kit
Applicant
BD BECTON DICKINSON VACUTAINER SYSTEMS PREANALYTIC
ONE BECTON DR.
FRANKLIN LAKES, NJ 07417-1880 US
Other 510(k) Applications for this Company
Contact
GREGORY W MORGAN
Other 510(k) Applications for this Contact
Regulation Number
868.5140
More FDA Info for this Regulation Number
Classification Product Code
CAZ
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
10/30/1995
Decision Date
05/20/1996
Decision
SESK - SUBST EQUIV - KIT
Classification Advisory Committee
AN - Anesthesiology
Review Advisory Committee
AN - Anesthesiology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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