K-number	K242102
Device name	CerroZone Mini
Applicant	Cerrozone, LLC
Product code	FRF
Device class	Class II
Decision date	Nov 19, 2024
Decision	Substantially Equivalent
Regulation	880.5045

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Source

View the full FDA submission: accessdata.fda.gov

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CerroZone Mini

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