FDA 510(k) Application Details - K150625

Device Classification Name	Instrument, Biopsy   More FDA Info for this Device
510(K) Number	K150625
Device Name	Instrument, Biopsy
Applicant	APRIOMED AB VIRDINGS ALLE' 28 UPPSALA 75450 SE Other 510(k) Applications for this Company
Contact	Bruno Edling 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	03/11/2015
Decision Date	06/09/2015
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