Chase Medical, Inc. - FDA 510(k) Cleared Devices
27
Total
27
Cleared
0
Denied
Chase Medical, Inc. has 27 FDA 510(k) cleared cardiovascular devices. Based in Richardson, US.
Historical record: 27 cleared submissions from 1997 to 2004.
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 Chase Medical, Inc.
27 devices
Cleared
Feb 02, 2004
CHASE CARDIAC ANALYSIS SYSTEM
Radiology
171d
Cleared
Sep 20, 2002
CHASE CARDIOVASCULAR PATCH KIT
Cardiovascular
85d
Cleared
Jun 03, 2002
CHARE CARIOVASCULAR PATCH
Cardiovascular
56d
Cleared
Mar 14, 2002
CHASE CARDIOVASCULAR PATCH KIT
Cardiovascular
50d
Cleared
Feb 26, 2002
CHASE CARDIOVASCULAR PATCH KIT
Cardiovascular
42d
Cleared
Aug 10, 2001
CHASE CARDIOVASCULAR PATCH
Cardiovascular
24d
Cleared
Jan 29, 2001
CHASE CARDIOVASCULAR PATCH
Cardiovascular
82d
Cleared
Aug 02, 2000
CHASE CARDIOVASCULAR PATCH
Cardiovascular
63d
Cleared
Mar 31, 1998
CHASE FEMORAL ACCESS CANNULATION SET
Cardiovascular
231d
Cleared
Jan 06, 1998
CHASE ANASTOMOSIS VISUALIZATION DEVICE
General Hospital
32d
Cleared
Oct 28, 1997
CHASE TEMPERATURE PROBE
Cardiovascular
222d
Cleared
Sep 08, 1997
CHASE THORACIC CATHETER
Cardiovascular
172d