K-number	K250264
Device name	SugarBug (1.x)
Applicant	Bench7, Inc.
Product code	MYN
Device class	Class II
Decision date	Nov 7, 2025
Decision	Substantially Equivalent
Regulation	892.2070

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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SugarBug (1.x)

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