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FDA 510(k) Application Details - K951870
Device Classification Name
Anesthesia Conduction Kit
More FDA Info for this Device
510(K) Number
K951870
Device Name
Anesthesia Conduction Kit
Applicant
INCUTECH, INC.
307-A SOUTH WESTGATE DR.
GREENSBORO, NC 27407 US
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Contact
ROGER V MOLINA
Other 510(k) Applications for this Contact
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
04/21/1995
Decision Date
01/22/1996
Decision
SESK - SUBST EQUIV - KIT
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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