FDA 510(k)

V•Stick™ Vascular Access Set

Número K: K253741 · 2025-12-15

Data da decisão2025-12-15

Código do produtoDYB

Comité consultivoCV

DecisãoSubstantially Equivalent

Resumo do dispositivo

V•Stick™ Vascular 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 2025-12-15 under 510(k) number K253741. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the V•Stick™ Vascular Access Set?

V•Stick™ Vascular Access Set is a medical device that received FDA 510(k) clearance on 2025-12-15. The listed applicant is Argon Medical Devices, Inc.. The 510(k) number is K253741.

When did V•Stick™ Vascular Access Set receive FDA 510(k) clearance?

V•Stick™ Vascular Access Set received FDA 510(k) clearance on 2025-12-15, under 510(k) number K253741.

Who is the listed applicant for V•Stick™ Vascular 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 V•Stick™ Vascular Access Set?

The FDA product code for V•Stick™ Vascular Access Set is DYB.

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Fonte oficial

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