CellMax Life’s Cancer Blood Test Designated FDA Breakthrough Device

Molecular diagnostics company CellMax Life’s FirstSight pre-cancer and cancer detection blood test has received the FDA’s Breakthrough Device designation.

The test is designed to detect and measure colorectal neoplasia-associated epithelial cells and DNA markers in human blood. The results, combined with age and gender, are integrated into a proprietary algorithm to generate a result of either low or high-risk for advanced neoplasia.

The test runs on the Sunnyvale, Calif.-based company’s proprietary platform for detecting cancer and pre-cancer.

August 30, 2021

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