FDA 510(k) Application Details - K001132

Device Classification Name	Instrument, Biopsy   More FDA Info for this Device
510(K) Number	K001132
Device Name	Instrument, Biopsy
Applicant	PROMEX, INC. 3049 HUDSON ST. FRANKLIN, IN 46131 US Other 510(k) Applications for this Company
Contact	JOSEPH L MARK Other 510(k) Applications for this Contact
Regulation Number	876.1075   More FDA Info for this Regulation Number
Classification Product Code	KNW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/10/2000
Decision Date	05/01/2000
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review