FDA 510(k) Application Details - K103302

Device Classification Name	Media, Culture, Ex Vivo, Tissue And Cell   More FDA Info for this Device
510(K) Number	K103302
Device Name	Media, Culture, Ex Vivo, Tissue And Cell
Applicant	LIFE TECHNOLOGIES CORPORATION 3175 STALEY ROAD GRAND ISLAND, NY 14072 US Other 510(k) Applications for this Company
Contact	KELLI TANZELLA Other 510(k) Applications for this Contact
Regulation Number	876.5885   More FDA Info for this Regulation Number
Classification Product Code	NDS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/09/2010
Decision Date	02/18/2011
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