FDA 510(k) Application Details - K020292

Device Classification Name	Cannula, Manipulator/Injector, Uterine   More FDA Info for this Device
510(K) Number	K020292
Device Name	Cannula, Manipulator/Injector, Uterine
Applicant	CATHETER RESEARCH, INC. 6131 WEST 80TH ST. INDIANAPOLIS, IN 46278 US Other 510(k) Applications for this Company
Contact	JOHN A STEEN 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	01/28/2002
Decision Date	04/17/2002
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