FDA 510(k) Application Details - K092983

Device Classification Name	Cannula, Manipulator/Injector, Uterine   More FDA Info for this Device
510(K) Number	K092983
Device Name	Cannula, Manipulator/Injector, Uterine
Applicant	Panpac Medical Corporation NO. 202, 6F-1.2, SEC.3 TATONG ROAD SHI-CHIH CITY, TAIPEI HSIEN 22103 TW Other 510(k) Applications for this Company
Contact	Yen-Ming Pan Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	LKF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/28/2009
Decision Date	06/07/2010
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