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FDA 510(k) Application Details - K052125
Device Classification Name
Insufflator, Laparoscopic
More FDA Info for this Device
510(K) Number
K052125
Device Name
Insufflator, Laparoscopic
Applicant
CARDIA INNOVATION AB
7307 GLOCHESTER DRIVE
EDINA, MN 55435 US
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Contact
JEFFREY R SHIDEMAN
Other 510(k) Applications for this Contact
Regulation Number
884.1730
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Classification Product Code
HIF
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More FDA Info for this Product Code
Date Received
08/05/2005
Decision Date
02/08/2006
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
OB - Obstetrics/Gynecology
Review Advisory Committee
OB - Obstetrics/Gynecology
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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