FDA 510(k) Application Details - K991424

Device Classification Name	Coagulator, Laparoscopic, Unipolar (And Accessories)   More FDA Info for this Device
510(K) Number	K991424
Device Name	Coagulator, Laparoscopic, Unipolar (And Accessories)
Applicant	MEDICOR CORP. 150 FAIRWAY DR. SUITE 164 VERNON HILLS, IL 60061 US Other 510(k) Applications for this Company
Contact	SCOTT B KERRIGAN Other 510(k) Applications for this Contact
Regulation Number	884.4160   More FDA Info for this Regulation Number
Classification Product Code	HFG Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/23/1999
Decision Date	07/22/1999
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