FDA 510(k) Application Details - K000974

Device Classification Name	Curette, Suction, Endometrial (And Accessories)   More FDA Info for this Device
510(K) Number	K000974
Device Name	Curette, Suction, Endometrial (And Accessories)
Applicant	UTAH MEDICAL PRODUCTS, INC. 7043 SOUTH 300 WEST MIDVALE, UT 84047-1048 US Other 510(k) Applications for this Company
Contact	KEVIN L CORNWELL Other 510(k) Applications for this Contact
Regulation Number	884.1175   More FDA Info for this Regulation Number
Classification Product Code	HHK Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/27/2000
Decision Date	05/23/2000
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