K-number	K252696
Device name	LEGACY
Applicant	Phasor Health, LLC
Product code	HBG
Device class	Class II
Decision date	Nov 21, 2025
Decision	Substantially Equivalent
Regulation	882.4300

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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LEGACY

Everything you need for a 510(k) submission. Nothing you don't.