FDA 510(k) Application Details - K955446

Device Classification Name	Cannula, Manipulator/Injector, Uterine   More FDA Info for this Device
510(K) Number	K955446
Device Name	Cannula, Manipulator/Injector, Uterine
Applicant	CONMED CORP. P.O. BOX 1408 DAYTON, OH 45401-1408 US Other 510(k) Applications for this Company
Contact	IRA D DUESLER, JR. 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	11/29/1995
Decision Date	06/18/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OB - Obstetrics/Gynecology
Review Advisory Committee	OB - Obstetrics/Gynecology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review