FDA 510(k) Application Details - K142791

Device Classification Name	Instrument, Biopsy   More FDA Info for this Device
510(K) Number	K142791
Device Name	Instrument, Biopsy
Applicant	SPECTRA MEDICAL DEVICES 260-F & H FORDHAM ROAD WILMINGTON, MA 01887 US Other 510(k) Applications for this Company
Contact	Agustin Turriza 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	09/26/2014
Decision Date	01/21/2015
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