Lsi Intl., Inc. is one of 7579 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lsi Intl., Inc. - FDA 510(k) Cleared Devices
Recent clearances: S.P. 100
5
Total
5
Cleared
0
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.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Lsi Intl., Inc.
5 devices