Medical Device Manufacturer · US , San Diego , CA

Sequenom, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2014

Total

Cleared

Denied

Sequenom, Inc. has 1 FDA 510(k) cleared medical devices. Based in San Diego, US.

Historical record: 1 cleared submissions from 2014 to 2014. Primary specialty: Pathology.

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

FDA 510(k) Regulatory Record - Sequenom, Inc.

1 devices

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