FDA 510(k) Application Details - K993801

Device Classification Name	Laparoscope, Gynecologic (And Accessories)   More FDA Info for this Device
510(K) Number	K993801
Device Name	Laparoscope, Gynecologic (And Accessories)
Applicant	ETHICON, INC. ROUTE 22 WEST P.O. BOX 151 SOMERVILLE, NJ 08876-0151 US Other 510(k) Applications for this Company
Contact	GREGORY R JONES Other 510(k) Applications for this Contact
Regulation Number	884.1720   More FDA Info for this Regulation Number
Classification Product Code	HET Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/09/1999
Decision Date	02/07/2000
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