FDA 510(k) Applications Submitted by GREINER BIO-ONE VACUETTE NORTH AMERICA

FDA 510(k) Number Submission Date Device Name Applicant
K011699 06/01/2001 VACUETTE EVACUATED BLOOD COLLECTION TUBES GREINER BIO-ONE VACUETTE NORTH AMERICA
K042927 10/22/2004 VACUETTE EDTA K3 EVACUATED BLOOD COLLECTION TUBES GREINER BIO-ONE VACUETTE NORTH AMERICA
K033478 11/03/2003 VACUETTE QUICKSHIELD SAFETY TUBE HOLDER GREINER BIO-ONE VACUETTE NORTH AMERICA
K023971 11/29/2002 VACUETTE TRACE ELEMENTS TUBES GREINER BIO-ONE VACUETTE NORTH AMERICA
K080235 01/30/2008 SAFETY INFUSION SET GREINER BIO-ONE VACUETTE NORTH AMERICA


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