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The increased concentration of GLP-1 produced leads to reductions in prandial glucose excursions

We are finalizing approval for device pass-through payment status for VasQ TM under the alternative pathway for devices that have an FDA Breakthrough Device designation and FDA marketing authorization for the indication for which the device has Breakthrough Device designation

Key considerations include: Lack of standardized dosing guidelines Limited long-term safety data Variability in manufacturing quality Anyone considering experimental therapies should do so under appropriate medical guidance

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