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FDA 510(k)

Scorpion Stylet Portal Vein Access Set, Scorpion Needle Portal Vein Access Set

N.º K: K202141 · 2021-01-15

SolicitanteArgon Medical Devices, Inc.
Fecha de decisión2021-01-15
Código de productoDYB
Comité asesorCV
DecisiónSubstantially Equivalent

Resumen del dispositivo

Scorpion Stylet Portal Vein Access Set, Scorpion Needle Portal Vein Access Set 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 2021-01-15 under 510(k) number K202141. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Scorpion Stylet Portal Vein Access Set, Scorpion Needle Portal Vein Access Set?

Scorpion Stylet Portal Vein Access Set, Scorpion Needle Portal Vein Access Set is a medical device that received FDA 510(k) clearance on 2021-01-15. The listed applicant is Argon Medical Devices, Inc.. The 510(k) number is K202141.

When did Scorpion Stylet Portal Vein Access Set, Scorpion Needle Portal Vein Access Set receive FDA 510(k) clearance?

Scorpion Stylet Portal Vein Access Set, Scorpion Needle Portal Vein Access Set received FDA 510(k) clearance on 2021-01-15, under 510(k) number K202141.

Who is the listed applicant for Scorpion Stylet Portal Vein Access Set, Scorpion Needle Portal Vein Access Set?

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 Scorpion Stylet Portal Vein Access Set, Scorpion Needle Portal Vein Access Set?

The FDA product code for Scorpion Stylet Portal Vein Access Set, Scorpion Needle Portal Vein Access Set is DYB.

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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.

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