Greiner Bio-One Vacuette North America

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K080235SAFETY INFUSION SETApril 24, 2008
K042927VACUETTE EDTA K3 EVACUATED BLOOD COLLECTION TUBESApril 15, 2005
K033478VACUETTE QUICKSHIELD SAFETY TUBE HOLDERDecember 29, 2003
K023971VACUETTE TRACE ELEMENTS TUBESJanuary 27, 2003
K011699VACUETTE EVACUATED BLOOD COLLECTION TUBESJune 28, 2001