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FDA 510(k) Application Details - K063282
Device Classification Name
Anesthesia Conduction Kit
More FDA Info for this Device
510(K) Number
K063282
Device Name
Anesthesia Conduction Kit
Applicant
B. BRAUN MEDICAL, INC.
901 MARCON BLVD.
ALLENTOWN, PA 18109-9341 US
Other 510(k) Applications for this Company
Contact
REBECCA STOLARICK
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
10/31/2006
Decision Date
06/20/2007
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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