Medical Device Manufacturer · US , Mchenry , IL

Harris-Lake, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1976

Total

Cleared

Denied

Harris-Lake, Inc. has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 7 cleared submissions from 1976 to 1977. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Harris-Lake, Inc.

7 devices

1-7 of 7