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US FDA Grants XVIVO Approval to Include DCD Hearts in IDE Clinical

US FDA Grants XVIVO Approval to Include DCD Hearts in IDE Clinical
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US FDA Grants XVIVO Approval to Include DCD Hearts in IDE Clinical Trial

25.07.2023 - GOTHENBURG, SWEDEN / ACCESSWIRE / July 25, 2023 / XVIVO Perfusion AB (STO:XVIVO)(LSE:0RKL)(FRA:3XV) The US Food & Drug Administration (FDA) has approved XVIVO s Investigational Device Exemption (IDE) supplement for its heart preservation clinical .

XVIVO has decided to close the PrimECC(R) Study for Further Patient Inclusions - Strategic Opportunities will be Evaluated

XVIVO has decided to close the PrimECC(R) Study for Further Patient Inclusions - Strategic Opportunities will be Evaluated
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XVIVO Perfusion AB: XVIVO has decided to close the PrimECC Study for Further Patient Inclusions - Strategic Opportunities will be Evaluated

XVIVO Perfusion AB: XVIVO has decided to close the PrimECC Study for Further Patient Inclusions - Strategic Opportunities will be Evaluated
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