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FDA 510(k) Application Details - K960619
Device Classification Name
Anesthesia Conduction Kit
More FDA Info for this Device
510(K) Number
K960619
Device Name
Anesthesia Conduction Kit
Applicant
INCUTECH, INC.
307-A SOUTH WESTGATE DR.
GREENSBORO, NC 27407 US
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Contact
ROGER MOLINA
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Regulation Number
868.5140
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Classification Product Code
CAZ
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More FDA Info for this Product Code
Date Received
02/13/1996
Decision Date
06/20/1996
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
AN - Anesthesiology
Review Advisory Committee
AN - Anesthesiology
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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