K-numberK253478
Device nameMotive™ Muscle Stimulator for Lower Back (OT01-1003)
ApplicantMotive Health, Inc.
Product codeNGX
Device classClass II
Decision dateNov 6, 2025
DecisionSubstantially Equivalent
Regulation890.5850
AI Summary

The FDA summary PDF for this submission is not available in machine-readable form — common for older clearances. View on FDA's site →

Source

View the full FDA submission: accessdata.fda.gov

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