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FDA 510(k) Application Details - K093556
Device Classification Name
Cannula, Manipulator/Injector, Uterine
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510(K) Number
K093556
Device Name
Cannula, Manipulator/Injector, Uterine
Applicant
CONMED CORPORATION
525 FRENCH RD.
UTICA, NY 13502 US
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Contact
SARAH RIZK
Other 510(k) Applications for this Contact
Regulation Number
000.0000
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Classification Product Code
LKF
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
11/17/2009
Decision Date
03/12/2010
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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