FDA 510(k) Application Details - K982999

Device Classification Name	Tubes, Vials, Systems, Serum Separators, Blood Collection   More FDA Info for this Device
510(K) Number	K982999
Device Name	Tubes, Vials, Systems, Serum Separators, Blood Collection
Applicant	GREINER MEDITECH, INC. 260 GATEWAY DRIVE, SUITE 17A BEL AIR, MD 21014 US Other 510(k) Applications for this Company
Contact	DOUG HARRIS Other 510(k) Applications for this Contact
Regulation Number	862.1675   More FDA Info for this Regulation Number
Classification Product Code	JKA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/27/1998
Decision Date	10/16/1998
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CH - Clinical Chemistry
Review Advisory Committee	CH - Clinical Chemistry
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review