Medical Device Manufacturer · US , Dallas , TX

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

1 submissions · 0 cleared · Since 2000

Total

Cleared

Denied

Ilife Systems, Inc. has 0 FDA 510(k) cleared medical devices. Based in Dallas, US.

Historical record: 0 cleared submissions from 2000 to 2000. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Ilife Systems, Inc.

1 devices

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