FDA 510(k)

Halo™ Single-Loop Snare Kit

N.º K: K200268 · 2020-06-03

Fecha de decisión2020-06-03

Código de productoMMX

Comité asesorCV

DecisiónSubstantially Equivalent

Resumen del dispositivo

Halo™ Single-Loop Snare 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 2020-06-03 under 510(k) number K200268. The device is classified under product code MMX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Halo™ Single-Loop Snare Kit?

Halo™ Single-Loop Snare Kit is a medical device that received FDA 510(k) clearance on 2020-06-03. The listed applicant is Argon Medical Devices, Inc.. The 510(k) number is K200268.

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

Halo™ Single-Loop Snare Kit received FDA 510(k) clearance on 2020-06-03, under 510(k) number K200268.

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

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

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Dispositivos relacionados (Código: MMX)

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Fuente oficial

Ver en la base de datos de la FDA →

Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.