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FDA 510(k)

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

K-Number: K191758 · 2019-12-17

ApplicantArgon Medical Devices, Inc.
Decision Date2019-12-17
Product CodeMMX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit is a medical device manufactured by Argon Medical Devices, Inc.. It received FDA 510(k) clearance on 2019-12-17 under approval number K191758. The device is classified under product code MMX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit?

Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit is a medical device that received FDA 510(k) clearance on 2019-12-17. It is manufactured by Argon Medical Devices, Inc.. The 510(k) number is K191758.

When was Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit approved by the FDA?

Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit received FDA 510(k) clearance on 2019-12-17, under approval number K191758.

What company makes Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit?

Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit is manufactured by Argon Medical Devices, Inc..

What is the FDA product code for Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit?

The FDA product code for Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit is MMX.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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