FDA 510(k) Applications Submitted by GREINER BIO-ONE NORTH AMERICA, INC.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K061483	05/30/2006	VACUETTE VISIO PLUS BLOOD COLLECTION NEEDLES	GREINER BIO-ONE NORTH AMERICA, INC.
K081929	07/07/2008	VACUETTE BLOOD COLLECTION TUBE WITH CLOT ACTIVATOR AND GEL SEPARATOR	GREINER BIO-ONE NORTH AMERICA, INC.
K072320	08/20/2007	GREINER VACUETTE QUICKSHIELD COMPLETE	GREINER BIO-ONE NORTH AMERICA, INC.
K122687	09/04/2012	BLOOD CULTURE HOLDER	GREINER BIO-ONE NORTH AMERICA, INC.
K102774	09/24/2010	VACUETTE QUICKSHIELD WITH SNAPPY TUDE HOLDER	GREINER BIO-ONE NORTH AMERICA, INC.
K103041	10/14/2010	VACUETTE BLOOD COLLECTION TUBE WITH LITHIUM HEPARIN AND GEL SEPARATOR	GREINER BIO-ONE NORTH AMERICA, INC.
K063357	11/07/2006	MINICOLLECT CAPILLARY BLOOD COLLECTION TUBES	GREINER BIO-ONE NORTH AMERICA, INC.
K113505	11/28/2011	VACUETTE QUICKSHIELD WITH SNAPPY TUBE HOLDER	GREINER BIO-ONE NORTH AMERICA, INC.
K121908	06/29/2012	SAFETY INFUSION SET	GREINER BIO-ONE NORTH AMERICA, INC.