Medical Device Manufacturer · US , Walker , MI

Wright Linear Pump, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1983

Recent clearances: WRIGHT MODEL 51 AND 52 SEQUENTIAL COMPRESSION SYSTEMS, WLP SEQUENTIAL VERSION MODEL WLP SOLO VI, WLP SOLO SEQUENTIAL, WLP GRADIENT SEQUENTIAL VERSION/WLP PROLITE/WLP WLP-II LITE

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.

510(k) submissions have been managed by Citech as regulatory consultant.

FDA 510(k) Regulatory Record - Wright Linear Pump, Inc.

6 devices
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