Medical Device Manufacturer · US , Walker , MI

Lifeline Systems, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1983

Total

Cleared

Denied

Lifeline Systems, Inc. has 4 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 4 cleared submissions from 1983 to 2010. Primary specialty: Cardiovascular.

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

Lifeline Systems, 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 - Lifeline Systems, Inc.

4 devices

1-4 of 4