ClearanceBrief
Company ยท DE

Carefusion Germany 234 GmbH

FDA 510(k) clearances and medical device recalls filed under this name, 2010 to 2016. Name variants (Inc, Corp, punctuation) are merged.

12510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
BZGSpirometer, Diagnostic4
BTYCalculator, Predicted Values, Pulmonary Function3
BZCCalculator, Pulmonary Function Data2
CAHFilter, Bacterial, Breathing-Circuit1
DQAOximeter1
DQKComputer, Diagnostic, Programmable1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Sep 16, 2016K153654Sentry WEB SmartInterp
Carefusion Germany 234 GmbH, DE
DQK
Aug 14, 2015K150810Vyntus / SentrySuite Product Line
Carefusion Germany 234 GmbH, DE
BZC
Mar 20, 2015K142959Vyntus Walk
Carefusion Germany 234 GmbH, DE
DQA
Dec 29, 2014K141936MICROBLAB, MICROLOOP
Carefusion Germany 234 GmbH, DE
BZG
Aug 22, 2014K133925VYNTUS/ SENTRYSUITE PRODUCT LINE
Carefusion Germany 234 GmbH, DE
BZC
Nov 19, 2012K122699SENTRYSUITE PRODUCT LINE
Carefusion Germany 234 GmbH, DE
BTY
May 10, 2012K113813SENTRYSUITE PRODUCT LINE
Carefusion Germany 234 GmbH, DE
BTY
Apr 13, 2012K113096MICRO I
Carefusion Germany 234 GmbH, DE
BZG
Oct 17, 2011K111408MICROGARD II
Carefusion Germany 234 GmbH, DE
CAH
Aug 12, 2011K111053SENTRYSUITE PRODUCT LINE
Carefusion Germany 234 GmbH, DE
BTY
Feb 10, 2011K101873MASTERSCREEN IOS
Carefusion Germany 234 GmbH, DE
BZG
Jan 13, 2010K092890ASTHMA MONITOR AM3
Carefusion Germany 234 GmbH, DE
BZG

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
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