FDA 510(k)

Halo Single-Loop Microsnare Kit

Número K: K200963 · 2021-01-05

Data da decisão2021-01-05

Código do produtoMMX

Comité consultivoCV

DecisãoSubstantially Equivalent

Resumo do dispositivo

Halo Single-Loop Microsnare 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 2021-01-05 under 510(k) number K200963. 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 Halo Single-Loop Microsnare Kit?

Halo Single-Loop Microsnare Kit is a medical device that received FDA 510(k) clearance on 2021-01-05. The listed applicant is Argon Medical Devices, Inc.. The 510(k) number is K200963.

When did Halo Single-Loop Microsnare Kit receive FDA 510(k) clearance?

Halo Single-Loop Microsnare Kit received FDA 510(k) clearance on 2021-01-05, under 510(k) number K200963.

Who is the listed applicant for Halo Single-Loop Microsnare 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 Halo Single-Loop Microsnare Kit?

The FDA product code for Halo Single-Loop Microsnare Kit is MMX.

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Fonte oficial

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