Medrad, Inc. - FDA 510(k) Cleared Devices
Recent clearances: JETSTREAM XC 2.4/3.4, ANGIOJET ULTRA POWER PULSE KIT, JETSTREAM XC 2.4/3.4 SYSTEM
105
Total
105
Cleared
0
Denied
FDA 510(k) Regulatory Record - Medrad, Inc. Cardiovascular ✕
47 devices
Cleared
Aug 27, 2014
JETSTREAM XC 2.4/3.4
Cardiovascular
335d
Cleared
Jul 29, 2013
ANGIOJET ULTRA POWER PULSE KIT
Cardiovascular
165d
Cleared
CT
Apr 10, 2013
JETSTREAM XC 2.4/3.4 SYSTEM
Cardiovascular
30d
Cleared
CT
Oct 19, 2012
JETSTREAM NAVITUS L SYSTEM JEYSTREAM NAVITUS SYSTEM JETSTREAM G3 SF SYSTEM...
Cardiovascular
28d
Cleared
Jun 06, 2012
ANGIOJET SOLENT DISTA THROMBECTOMY SET
Cardiovascular
204d
Cleared
Dec 15, 2011
MEDRAD MARK 7 ARTERION (PEDESTAL SYSTEM), (TABLE MOUNT SYSTEM), MEDRAD MARK 7...
Cardiovascular
52d
Cleared
Dec 02, 2011
ANGIOJET ULTRA DVX THROMBECTOMY SET
Cardiovascular
11d
Cleared
Oct 14, 2011
MEDRAD MARK 7 ARTERION (PEDESTAL SYSTEM / TABLE MOUNT SYSTEM), MEDRAD MARK 7...
Cardiovascular
85d
Cleared
May 24, 2011
ANGIOJET SOLENT OMNI THROMBECTOMY SET
Cardiovascular
27d
Cleared
Jan 12, 2009
MEDRAD STELLANT CT INJECTOR SYSTEM WITH P3T CARDIAC
Cardiovascular
104d
Cleared
Dec 21, 2007
MEDRAD STELLANT CT INJECTOR SYSTEM WITH P3T
Cardiovascular
73d
Cleared
Mar 27, 2007
MEDRAD STELLANT CT INJECTOR SYSTEM WITH XDS ACCESSORY
Cardiovascular
168d
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