Medical Device Manufacturer · US , Grand Island , NY

Life Technologies, Inc. - FDA 510(k) Cleared Devices

4 submissions · 3 cleared · Since 1995

Total

Cleared

Denied

Life Technologies, Inc. has 3 FDA 510(k) cleared medical devices. Based in Grand Island, US.

Historical record: 3 cleared submissions from 1995 to 2012. Primary specialty: Obstetrics & Gynecology.

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

FDA 510(k) Regulatory Record - Life Technologies, Inc.

4 devices

1-4 of 4