FDA 510(k) Application Details - K970151

Device Classification Name	Laparoscope, Gynecologic (And Accessories)   More FDA Info for this Device
510(K) Number	K970151
Device Name	Laparoscope, Gynecologic (And Accessories)
Applicant	SMITH & NEPHEW, INC. 130 FORBES BLVD. MANSFIELD, MA 02048 US Other 510(k) Applications for this Company
Contact	SUSAN A FINNERAN 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	01/15/1997
Decision Date	03/18/1997
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