FDA Grants Breakthrough Device Designation to MeMed Severity Test for Patients with Suspected Sepsis

FDA Grants Breakthrough Device Designation to MeMed Severity Test for 
Patients with Suspected Sepsis

This designation advances the management of acute infections and sepsis by empowering clinicians with timely insights for better patient...
1 week ago
from: Business Wire

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Food and Drug Administration, Medicine, Sepsis
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