K-number	K252060
Device name	GREEN
Applicant	Phasor Health, LLC
Product code	HBE
Device class	Class II
Decision date	Oct 31, 2025
Decision	Substantially Equivalent
Regulation	882.4310

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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GREEN

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