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

FDA 510(k) Number Submission Date Device Name Applicant
K011786 06/08/2001 VACUETTE SAFETY BLOOD COLLECTION SET GREINER VACUETTE NORTH AMERICA, INC.
K012043 06/29/2001 VACUETTE EDTA K2 GEL TUBES GREINER VACUETTE NORTH AMERICA, INC.
K002777 09/06/2000 VACUETTE WITH PPACK GREINER VACUETTE NORTH AMERICA, INC.
K003812 12/11/2000 VACUETTE SPEEDY QUICK-RELEASE HOLDER GREINER VACUETTE NORTH AMERICA, INC.
K014104 12/13/2001 VACUETTE EDTA K2 TUBES GREINER VACUETTE NORTH AMERICA, INC.


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