FDA 510(k) Application Details - K141894

Device Classification Name	Kit, Needle, Biopsy   More FDA Info for this Device
510(K) Number	K141894
Device Name	Kit, Needle, Biopsy
Applicant	COVIDIEN LLC (FORMERLY BEACON ENDOSCOPIC CORP) 2000 COMMONWEALTH AVE. SUITE 110 AUBURNDALE, MA 02466-2008 US Other 510(k) Applications for this Company
Contact	Saket Bhatt Other 510(k) Applications for this Contact
Regulation Number	876.1075   More FDA Info for this Regulation Number
Classification Product Code	FCG Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/14/2014
Decision Date	10/06/2014
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