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Carefusion Germany 234 GmbH

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
12
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K153654Sentry WEB SmartInterpSeptember 16, 2016
K150810Vyntus / SentrySuite Product LineAugust 14, 2015
K142959Vyntus WalkMarch 20, 2015
K141936MICROBLAB, MICROLOOPDecember 29, 2014
K133925VYNTUS/ SENTRYSUITE PRODUCT LINEAugust 22, 2014
K122699SENTRYSUITE PRODUCT LINENovember 19, 2012
K113813SENTRYSUITE PRODUCT LINEMay 10, 2012
K113096MICRO IApril 13, 2012
K111408MICROGARD IIOctober 17, 2011
K111053SENTRYSUITE PRODUCT LINEAugust 12, 2011
K101873MASTERSCREEN IOSFebruary 10, 2011
K092890ASTHMA MONITOR AM3January 13, 2010