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 |
|