K-number	DEN240062
Device name	Minder System
Applicant	Epi-Minder Pty, Ltd.
Product code	SEM
Device class	Class II
Decision date	Apr 17, 2025
Decision	Not Substantially Equivalent
Regulation	882.1360

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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Minder System

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