iRhythm Technologies Receives FDA 510(k) Clearance For Design Modifications To Zio AT Device
Portfolio Pulse from Benzinga Newsdesk
iRhythm Technologies has received FDA 510(k) clearance for design modifications to its Zio AT device, which is used for ambulatory Mobile Cardiac Telemetry (MCT) monitoring. The enhancements will be available in 2025.
October 30, 2024 | 9:16 pm
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iRhythm Technologies received FDA 510(k) clearance for design modifications to its Zio AT device, enhancing its MCT monitoring capabilities. These enhancements are expected to be available in 2025.
The FDA clearance is a positive regulatory milestone for iRhythm Technologies, likely to enhance its product offering and market position in the MCT monitoring space. This could lead to increased investor confidence and potential stock price appreciation.
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