FDA 510(k) Applications Submitted by CareFusion Germany 234 GmbH

FDA 510(k) Number Submission Date Device Name Applicant
K092890 09/21/2009 ASTHMA MONITOR AM3 CAREFUSION GERMANY 234 GMBH
K150810 03/26/2015 Vyntus / SentrySuite Product Line CareFusion Germany 234 GmbH
K111053 04/15/2011 SENTRYSUITE PRODUCT LINE CAREFUSION GERMANY 234 GMBH
K111408 05/19/2011 MICROGARD II CAREFUSION GERMANY 234 GMBH
K101873 07/06/2010 MASTERSCREEN IOS CAREFUSION GERMANY 234 GMBH
K141936 07/17/2014 MICROBLAB, MICROLOOP CAREFUSION GERMANY 234 GMBH
K122699 09/04/2012 SENTRYSUITE PRODUCT LINE CAREFUSION GERMANY 234 GMBH
K142959 10/14/2014 Vyntus Walk CAREFUSION GERMANY 234 GMBH
K113096 10/19/2011 MICRO I CAREFUSION GERMANY 234 GMBH
K153654 12/21/2015 Sentry WEB SmartInterp CareFusion Germany 234 GmbH
K113813 12/23/2011 SENTRYSUITE PRODUCT LINE CAREFUSION GERMANY 234 GMBH
K133925 12/23/2013 VYNTUS/ SENTRYSUITE PRODUCT LINE CAREFUSION GERMANY 234 GMBH


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