FDA 510(k) Applications Submitted by Helix OpCo, LLC

FDA 510(k) Number Submission Date Device Name Applicant
DEN190035 08/02/2019 Helix Laboratory Platform Helix OpCo, LLC
K192073 08/02/2019 Helix Genetic Health Risk App for late-onset AlzheimerÆs disease Helix OpCo, LLC


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