FDA 510(k) Applications Submitted by GREINER AMERICA, INC.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K960857	03/01/1996	GREINER VACUETTE BLOOD COLLECTION TUBE W/LITHIUM HEPARIN & GEL SEPARATOR	GREINER AMERICA, INC.
K960858	03/01/1996	GREINER VACUTTE BLOOD COLLECTION TUBE W/ CLOT ACTIVATOR & GEL SEPARATOR	GREINER AMERICA, INC.
K960860	03/01/1996	GREINER VACUETTE BLOOD COLLECTION TUBE E/EDTA K3	GREINER AMERICA, INC.
K971220	04/02/1997	GREINER VACUETTE BLOOD COLLECTION TUBE	GREINER AMERICA, INC.
K971221	04/02/1997	GREINER VACUETTE BLOOD COLLECTION TUBE	GREINER AMERICA, INC.
K971236	04/02/1997	GREINER VACUETTE BLOOD COLLECTION TUBE	GREINER AMERICA, INC.
K971239	04/02/1997	GREINER VACUETTE BLOOD COLLECTION TUBE	GREINER AMERICA, INC.