FDA 510(k)

AV Vascular

Número K: K253735 · 2026-01-22

RequerentePhilips Medical Systems Nederland B.V.

Data da decisão2026-01-22

Código do produtoQIH

Comité consultivoRA

DecisãoSubstantially Equivalent

Resumo do dispositivo

AV Vascular is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems Nederland B.V.. It received FDA 510(k) clearance on 2026-01-22 under 510(k) number K253735. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the AV Vascular?

AV Vascular is a medical device that received FDA 510(k) clearance on 2026-01-22. The listed applicant is Philips Medical Systems Nederland B.V.. The 510(k) number is K253735.

When did AV Vascular receive FDA 510(k) clearance?

AV Vascular received FDA 510(k) clearance on 2026-01-22, under 510(k) number K253735.

Who is the listed applicant for AV Vascular?

The FDA 510(k) record lists Philips Medical Systems Nederland B.V. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AV Vascular?

The FDA product code for AV Vascular is QIH.

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Fonte oficial

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