Oscor, Inc. - FDA 510(k) Cleared Devices
49
Total
46
Cleared
0
Denied
Oscor, Inc. has 46 FDA 510(k) cleared cardiovascular devices. Based in Palm Harbor, US.
Last cleared in 2021. Active since 1979.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Oscor, Inc.
49 devices
Cleared
Jun 03, 2021
Breezeway II
Cardiovascular
93d
Cleared
Sep 22, 2015
Destino Reach
Cardiovascular
69d
Cleared
Mar 19, 2015
IS4/DF4 Port Plug
Cardiovascular
105d
Cleared
Jul 09, 2014
INTRODUCER, MODEL ADELANTE MAGNUM
Cardiovascular
90d
Cleared
Apr 17, 2014
DESTINO TWIST, STEERABLE GUIDING SHEATH
Cardiovascular
58d
Cleared
Feb 13, 2014
INTRODUCER SETS, MODEL ADELANTE RADIAL
Cardiovascular
339d
Cleared
Jan 08, 2014
SAFESEPT NEEDLE FREE TRANSSEPTAL TROCAR GUIDEWIRE
Cardiovascular
287d
Cleared
Jun 13, 2013
GUIDEWIRE, PURSUER SERIES
Cardiovascular
149d
Cleared
Dec 13, 2012
DELIVERY SHEATH, MODEL ADELANTE BREEZEWAY
Cardiovascular
79d
Cleared
Dec 13, 2012
STEERABLE GUIDING SHEATH, MODEL ADELANTE DESTINO
Cardiovascular
79d
Cleared
Aug 29, 2012
INTRODUCER SET, MODEL ADELANTE-S SERIES
Cardiovascular
44d
Cleared
Jun 29, 2012
STEERABLE GUIDING SHEATH, MODEL ADELANTE DESTINO
Cardiovascular
135d
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