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FDA 510(k) Application Details - K954706
Device Classification Name
Anesthesia Conduction Kit
More FDA Info for this Device
510(K) Number
K954706
Device Name
Anesthesia Conduction Kit
Applicant
KENDALL HEALTHCARE PRODUCTS CO. DIV.OF TYCO HEALTH
15 HAMPSHIRE ST.
MANSFIELD, MA 02048 US
Other 510(k) Applications for this Company
Contact
DAVID A OLSON
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
10/12/1995
Decision Date
05/30/1996
Decision
SESD - SUBST EQUIV - WITH DRUG
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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