Medical Device Manufacturer · US , San Diego , CA

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

1 submissions · 1 cleared · Since 2014

Official Website

1

Total

1

Cleared

0

Denied

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

1 devices

1-1 of 1

Cleared Jun 13, 2014

IMPACT DX FACTOR V LEIDEN AND FACTOR II GENOTYPING TEST

Pathology · 263d