Osprey Medical, Inc. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Osprey Medical, Inc. has 14 FDA 510(k) cleared cardiovascular devices. Based in Eden Prairie, US.
Historical record: 14 cleared submissions from 2013 to 2019.
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 Osprey Medical, Inc.
14 devices
Cleared
Oct 17, 2019
DyeVert™ Plus Contrast Reduction System, DyeTect™ Contrast Monitoring System,...
General Hospital
268d
Cleared
Dec 20, 2018
DyeVert™ NG Contrast Reduction System, DyeVert™ PLUS EZ Contrast Reduction...
Cardiovascular
27d
Cleared
Oct 25, 2018
DyeVert PLUS EZ Contrast Reduction System
Cardiovascular
98d
Cleared
Jul 07, 2017
Smart Syringe
Cardiovascular
29d
Cleared
May 26, 2017
DyeVert Plus Contrast Reduction System, DyeVert NG Contrast Reduction System
Cardiovascular
30d
Cleared
Mar 08, 2017
DyeVert Plus Contrast Modulation/Monitoring System, Contrast Monitoring System
Cardiovascular
127d
Cleared
Aug 03, 2016
DyeVert NG Contrast Modulation System
Cardiovascular
63d
Cleared
Feb 04, 2016
DyeVert Contrast Modulation System
Cardiovascular
97d
Cleared
Oct 15, 2015
AVERT Contrast Modulation System
Cardiovascular
153d
Cleared
Oct 09, 2015
Dyevert Contrast Modulation System
Cardiovascular
102d
Cleared
Mar 26, 2015
AVERT Contrast Modulation System
Cardiovascular
30d
Cleared
Dec 12, 2014
CONTRAST MONITORING SYSTEM DISPLAY, CONTRAST MONITORING SYSTEM SYRINGES
Cardiovascular
134d