K-number	K191758
Device name	Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit
Applicant	Argon Medical Devices, Inc.
Product code	MMX
Device class	Class II
Decision date	Dec 17, 2019
Decision	Substantially Equivalent
Regulation	—

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Source

View the full FDA submission: accessdata.fda.gov

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Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit

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