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For additional information about ARM, regulatory positioning, partnership opportunities, or commercial discussions, please contact our team.
CONNECT WITH SMART MACHINES CORPORATION
What We Can Discuss
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Product information about the ARM system
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Clinical and rehabilitation use-case discussions
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Commercial and partnership inquiries
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Regulatory and quality overview questions
ARM is being positioned under FDA Product Code IKK, 21 CFR 890.1925, “isokinetic testing and evaluation system,” a Class II device category currently listed as 510(k) exempt, subject to applicable limitations and general controls.
General contact
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