FDA 510(k) Application Details - K022086

Device Classification Name	Media, Culture, Ex Vivo, Tissue And Cell   More FDA Info for this Device
510(K) Number	K022086
Device Name	Media, Culture, Ex Vivo, Tissue And Cell
Applicant	INVITROGEN CORPORATION 3175 STALEY RD. GRAND ISLAND, NY 14072 US Other 510(k) Applications for this Company
Contact	KEITH D GITTERMAN 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	06/27/2002
Decision Date	12/23/2002
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