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See today's BioWorld MedTech
Home » Cytovale gets FDA nod for 10-minute sepsis test
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Cytovale gets FDA nod for 10-minute sepsis test

Jan. 18, 2023
By Annette Boyle

Cytovale Inc. received U.S. FDA 510(k) clearance for its Intellisep sepsis test, which can aid in the diagnosis of the often fatal condition within 10 minutes. Cytovale is one of several companies and collaborations that aim to sharply reduce the time to diagnosis and the mortality rate for sepsis by providing quicker, more informative test results and standardizing protocols.

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