K-number	K200963
Device name	Halo Single-Loop Microsnare Kit
Applicant	Argon Medical Devices, Inc.
Product code	MMX
Device class	Class II
Decision date	Jan 5, 2021
Decision	Substantially Equivalent
Regulation	870.5150

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Source

View the full FDA submission: accessdata.fda.gov

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Halo Single-Loop Microsnare Kit

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