FDA 510(k) Application Details - K990387

Device Classification Name	Curette, Suction, Endometrial (And Accessories)   More FDA Info for this Device
510(K) Number	K990387
Device Name	Curette, Suction, Endometrial (And Accessories)
Applicant	U.A. MEDICAL PRODUCTS, INC. 9303-G2 MONROE RD. CHARLOTTE, NC 28270 US Other 510(k) Applications for this Company
Contact	FANISH ENGINEER 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	02/08/1999
Decision Date	04/20/1999
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