Carefusion Germany 234 GmbH is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Carefusion Germany 234 GmbH - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Carefusion Germany 234 GmbH has 12 FDA 510(k) cleared anesthesiology devices. Based in Hoechberg, DE.
Historical record: 12 cleared submissions from 2010 to 2016.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Carefusion Germany 234 GmbH
12 devices
Cleared
Sep 16, 2016
Sentry WEB SmartInterp
Cardiovascular
270d
Cleared
Aug 14, 2015
Vyntus / SentrySuite Product Line
Anesthesiology
141d
Cleared
Mar 20, 2015
Vyntus Walk
Anesthesiology
157d
Cleared
Dec 29, 2014
MICROBLAB, MICROLOOP
Anesthesiology
165d
Cleared
Aug 22, 2014
VYNTUS/ SENTRYSUITE PRODUCT LINE
Anesthesiology
242d
Cleared
Nov 19, 2012
SENTRYSUITE PRODUCT LINE
Anesthesiology
76d
Cleared
May 10, 2012
SENTRYSUITE PRODUCT LINE
Anesthesiology
139d
Cleared
Apr 13, 2012
MICRO I
Anesthesiology
177d
Cleared
Oct 17, 2011
MICROGARD II
General Hospital
151d
Cleared
Aug 12, 2011
SENTRYSUITE PRODUCT LINE
Anesthesiology
119d
Cleared
Feb 10, 2011
MASTERSCREEN IOS
Anesthesiology
219d
Cleared
Jan 13, 2010
ASTHMA MONITOR AM3
Anesthesiology
114d