Medical Device Manufacturer · US , Sandpoint , ID

Lead-Lok, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1989

Total

Cleared

Denied

Lead-Lok, Inc. has 5 FDA 510(k) cleared medical devices. Based in Sandpoint, US.

Historical record: 5 cleared submissions from 1989 to 2001. Primary specialty: Cardiovascular.

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

FDA 510(k) Regulatory Record - Lead-Lok, Inc.

5 devices

1-5 of 5