FDA 510(k) Application Details - K993777

Device Classification Name	Electrocautery, Gynecologic (And Accessories)   More FDA Info for this Device
510(K) Number	K993777
Device Name	Electrocautery, Gynecologic (And Accessories)
Applicant	R-GROUP INTL. 2321 N.W. 66TH CT., SUITE W-4 GAINESVILLE, FL 32653 US Other 510(k) Applications for this Company
Contact	KERRY A KAHN Other 510(k) Applications for this Contact
Regulation Number	884.4120   More FDA Info for this Regulation Number
Classification Product Code	HGI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/08/1999
Decision Date	05/25/2000
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