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FDA 510(k) Application Details - K113188
Device Classification Name
Anesthesia Conduction Kit
More FDA Info for this Device
510(K) Number
K113188
Device Name
Anesthesia Conduction Kit
Applicant
PAJUNK GMBH MEDIZINTECHNOLOGIE
KARL-HALL-STRASSE 1
GEISINGEN 78187 DE
Other 510(k) Applications for this Company
Contact
CHRISTIAN G QUASS
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
10/31/2011
Decision Date
03/01/2012
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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