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FDA 510(k) Application Details - K121525
Device Classification Name
Anesthesia Conduction Kit
More FDA Info for this Device
510(K) Number
K121525
Device Name
Anesthesia Conduction Kit
Applicant
SMITHS MEDICAL ASD, INC.
10 BOWMAN DR.
KEENE, NH 03431 US
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Contact
CHRISTINE LLOYD
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
05/23/2012
Decision Date
08/02/2012
Decision
SESE - SUBST EQUIV
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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