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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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