Medical Device Manufacturer · US , Arlington , VA

Longport, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1999

Total

Cleared

Denied

Longport, Inc. has 2 FDA 510(k) cleared medical devices. Based in Arlington, US.

Historical record: 2 cleared submissions from 1999 to 2006. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Longport, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Longport, Inc.

2 devices

1-2 of 2