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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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