FDA 510(k) Application Details - K014248

Device Classification Name	Instrument, Manual, Specialized Obstetric-Gynecologic   More FDA Info for this Device
510(K) Number	K014248
Device Name	Instrument, Manual, Specialized Obstetric-Gynecologic
Applicant	UROGYN LTD. DIAMOND BLDG.(26TH FL.) 3A JABOTINSKY ST. RAMAT-GAN 52520 IL Other 510(k) Applications for this Company
Contact	EREZ ADIV Other 510(k) Applications for this Contact
Regulation Number	884.4530   More FDA Info for this Regulation Number
Classification Product Code	KNA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/26/2001
Decision Date	03/21/2002
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