Codman & Shurtleff, Inc. - FDA 510(k) Cleared Devices
152
Total
151
Cleared
0
Denied
FDA 510(k) cleared devices by Codman & Shurtleff, Inc. Cardiovascular ✕
13 devices
Cleared
Jul 03, 2017
YOGA Microcatheter, 0.032, 150cm, Back Up and Extra Back Up
Cardiovascular
28d
Cleared
Jan 05, 2017
YOGA Microcatheter
Cardiovascular
113d
Cleared
Apr 24, 2014
ENVOY DISTAL ACCESS (DA) GUIDING CATHETER, 6F, 95CM & 105CM, STRAIGHT & XB,...
Cardiovascular
100d
Cleared
Apr 21, 2014
ENVOY GUIDING CATHETER
Cardiovascular
73d
Cleared
Aug 30, 2013
ReVive PV (Peripheral Vasculature) Thrombectomy Device
Cardiovascular
38d
Cleared
Aug 14, 2012
AGILITY STEERABLE GUIDEWIRE NEUROSCOUT STEERABLE GUDIEWIRE
Cardiovascular
57d
Cleared
Feb 24, 2012
ENVOY DISTAL ACCESS GUIDING CATHETER
Cardiovascular
30d
Cleared
Oct 25, 2011
REVIVE INTERMEDIATE CATHETER (REVIVE IC)
Cardiovascular
27d
Cleared
Mar 16, 2010
NEUROSCOUT STEERABLE GUIDEWIRE
Cardiovascular
32d
Cleared
Nov 06, 2009
ENVOY GUIDING CATHETERS
Cardiovascular
28d
Cleared
Nov 27, 1981
EPC FILTER
Cardiovascular
23d
Cleared
Jun 20, 1977
HUANG VEIN HOLDER, #21-8011
Cardiovascular
12d