FDA 510(k) Application Details - K001818

Device Classification Name	Tenaculum, Uterine   More FDA Info for this Device
510(K) Number	K001818
Device Name	Tenaculum, Uterine
Applicant	TOWNE BROTHERS (PVT.), LTD. 52-B INDUSTRIAL ESTATE P.O. BOX 108 SIALKOT 51310 PK Other 510(k) Applications for this Company
Contact	ABDUL GHAFOOR Other 510(k) Applications for this Contact
Regulation Number	884.4530   More FDA Info for this Regulation Number
Classification Product Code	HDC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/15/2000
Decision Date	08/30/2000
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