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Imricor hits key milestone in FDA approval process for ablation catheter devices

Summary by Stockhead
The second module for Imricor’s premarket approval products has been submitted to the US FDA Module two comprises manufacturing processes across seven devices and has been submitted within expected timelines Imricor’s 3D mapping and guidance system NorthStar will be submitted next under the 510(k) process   Special Report: Imricor Medical Systems has announced another key milestone towards US regulatory approval for its devices with submission o…

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abc broke the news in Spain on Monday, March 3, 2025.
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