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Greiner Vacuette North America, Inc.

FDA Regulatory Profile

Greiner Vacuette North America, Inc. appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on February 1, 2002.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K014104VACUETTE EDTA K2 TUBESFebruary 1, 2002
K012043VACUETTE EDTA K2 GEL TUBESSeptember 24, 2001
K011786VACUETTE SAFETY BLOOD COLLECTION SETJuly 12, 2001
K003812VACUETTE SPEEDY QUICK-RELEASE HOLDERApril 30, 2001
K002777VACUETTE WITH PPACKOctober 5, 2000

FDA data resources