FDA 510(k)

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

Número K: K191758 · 2019-12-17

Data da decisão2019-12-17

Código do produtoMMX

Comité consultivoCV

DecisãoSubstantially Equivalent

Resumo do dispositivo

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

Perguntas frequentes

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. The listed applicant is Argon Medical Devices, Inc.. The 510(k) number is K191758.

When did Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit receive FDA 510(k) clearance?

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

Who is the listed applicant for Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit?

The FDA 510(k) record lists Argon Medical Devices, Inc. as the applicant. This does not by itself establish the device manufacturer.

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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Fonte oficial

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