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2.9.21 - Cleveland Diagnostics, Inc. Raises Over $19 Million in Financing


1.13.21 - Publication of a Health Economic Analysis Demonstrates IsoPSA® Significantly Reduces Unnecessary Prostate Cancer Biopsies and Costs


10.16.19 - Cleveland Diagnostics Announces FDA Breakthrough Device Designation for Novel Prostate Cancer Diagnostic Test


5.7.19 - Cleveland Diagnostics Announces Publication of Multicenter IsoPSA Clinical Validation Study Demonstrating Improved Accuracy Over Prostate-Specific Antigen Test


5.15.17 - Cleveland Diagnostics Announces Preliminary Results from Multicenter IsoPSA™ Study Demonstrating Significantly Improved Accuracy Over Standard Prostate-Specific Antigen (PSA) Test

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This material concerns the IsoPSA Test, a laboratory developed test (LDT) from Cleveland Diagnostics, Inc., which is performed by CLIA-certified laboratories qualified to conduct high-complexity clinical testing and is only intended for use consistent with applicable CLIA requirements. When offered as an LDT, the IsoPSA Test has not been cleared or approved by the U.S. Food and Drug Administration (FDA).


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