Medical Device Manufacturer · US , San Leandro , CA

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

7 submissions · 7 cleared · Since 1990

Total

Cleared

Denied

Lumisys, Inc. has 7 FDA 510(k) cleared medical devices. Based in San Leandro, US.

Historical record: 7 cleared submissions from 1990 to 1998. Primary specialty: Radiology.

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

Lumisys, Inc. is one of 7681 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

7 devices

1-7 of 7