FDA 510(k) Application Details - K041544

Device Classification Name	Instrument, Biopsy   More FDA Info for this Device
510(K) Number	K041544
Device Name	Instrument, Biopsy
Applicant	UROLOGICAL INC. 1100 W. MORGAN STREET SPENCER, IN 47460 US Other 510(k) Applications for this Company
Contact	CINDY RUMPLE 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	06/09/2004
Decision Date	07/22/2004
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review