Wright Linear Pump, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Wright Linear Pump, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Wright Linear Pump, Inc. has 6 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 6 cleared submissions from 1983 to 2007. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Wright Linear Pump, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Wright Linear Pump, Inc.
6 devices
Cleared
May 22, 2007
WRIGHT MODEL 51 AND 52 SEQUENTIAL COMPRESSION SYSTEMS
Cardiovascular
40d
Cleared
Nov 06, 1996
WLP SEQUENTIAL VERSION MODEL WLP SOLO VI, WLP SOLO SEQUENTIAL
Cardiovascular
216d
Cleared
Nov 06, 1996
WLP GRADIENT SEQUENTIAL VERSION/WLP PROLITE/WLP WLP-II LITE
Cardiovascular
181d
Cleared
Nov 06, 1996
WLP SINGLE-SEGMENT VERSION WLP SOLO VII
Cardiovascular
181d
Cleared
Nov 21, 1988
WRIGHT GRADIENT PRESSURE SUPPORT STOCKINGS
General Hospital
116d
Cleared
May 25, 1983
LINEAR PUMP #4370975
Cardiovascular
91d