Medical Device Manufacturer · US , Overland Park , KS

Lsi Intl., Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1994

Total

Cleared

Denied

Lsi Intl., Inc. has 5 FDA 510(k) cleared medical devices. Based in Overland Park, US.

Historical record: 5 cleared submissions from 1994 to 2000. Primary specialty: Physical Medicine.

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

Lsi Intl., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Lsi Intl., Inc.

5 devices

1-5 of 5