In this episode, David West discusses Proscia's recent 510K clearance for Concentric AP-Dx software. The conversation delves into the significance of 510 k clearance, explaining its role in regulatory approval for medical devices.
David highlights the company's global success and previous clearances in Europe, offering insights into the journey of bringing innovative software to laboratories worldwide.
We discuss not only the importance of this clearance to Proscia, but also to digital pathology as a whole.
Links for this episode:
Proscia
Proscia Receives FDA 510(k) Clearance For Concentriq AP-Dx
Welcome To Concentriq AP-Dx Webinar
Health Podcast Network
LabVine Learning
Dress A Med scrubs
Digital Pathology Club
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