FDA 510(k) Application Details - K071907

Device Classification Name	Cannula, Manipulator/Injector, Uterine   More FDA Info for this Device
510(K) Number	K071907
Device Name	Cannula, Manipulator/Injector, Uterine
Applicant	CONMED CORPORATION 525 FRENCH RD. UTICA, NY 13502 US Other 510(k) Applications for this Company
Contact	BRIAN KILLORAN Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	LKF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/10/2007
Decision Date	10/05/2007
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OB - Obstetrics/Gynecology
Review Advisory Committee	OB - Obstetrics/Gynecology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review