FDA 510(k) Application Details - DEN000008

Device Classification Name	Media, Culture, Ex Vivo, Tissue And Cell   More FDA Info for this Device
510(K) Number	DEN000008
Device Name	Media, Culture, Ex Vivo, Tissue And Cell
Applicant	LIFE TECHNOLOGIES, INC. 555 THIRTEENTH STREET, N.W. WASHINGTON, DC 20004-1109 US Other 510(k) Applications for this Company
Contact	JONATHAN S KAHAN, ESQ. 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	12/19/2000
Decision Date	02/16/2001
Decision	DENG -
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status
Type	Post-NSE
Reviewed By Third Party	N
Expedited Review