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BioCardia Announces Japan PMDA Record Of Advice Supports Regulatory Submission For Approval Of CardiAMP Cell Therapy For Ischemic Heart Failure

Submission Anticipated in Q4 2026SUNNYVALE, Calif., May 28, 2026 (GLOBE NEWSWIRE) -- BioCardia®, Inc. [Nasdaq: BCDA], a global leader in cellular and cell-derived therapeutics for the treatment of cardiovascular and pulmonary diseases, today reported the Consultation Record from Japan’s Pharmaceutical and Medical Device Agency (PMDA) supports submission for regulatory approval of the CardiAMP® cell therapy for the treatment of ischemic heart failure of reduced ejection fraction (HFrEF) based on

articleBiocardia, Inc.May 28, 20264/company/biocardia-inc/news/biocardia-announces-japan-pmda-record-of-advice-supports-regulatory-submission-for-approval-of-cardiamp-cell-therapy-for-ischemic-heart-failure
BioCardia Announces Japan PMDA Record Of Advice Supports Regulatory Submission For Approval Of CardiAMP Cell Therapy For Ischemic Heart Failure

About this update from Biocardia, Inc.

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PMDABioCardiaregulatory approvalcell therapyJapanregulatory submissionpulmonary diseaseischemic heart failurepulmonary diseasesforward-looking statements