FDA 510(k)

Medline Reusable Blood Pressure Cuff

Número K: K254287 · 2026-06-22

Data da decisão2026-06-22

Código do produtoDXQ

Comité consultivoCV

DecisãoSubstantially Equivalent

Resumo do dispositivo

Medline Reusable Blood Pressure Cuff is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, LP. It received FDA 510(k) clearance on 2026-06-22 under 510(k) number K254287. The device is classified under product code DXQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Medline Reusable Blood Pressure Cuff?

Medline Reusable Blood Pressure Cuff is a medical device that received FDA 510(k) clearance on 2026-06-22. The listed applicant is Medline Industries, LP. The 510(k) number is K254287.

When did Medline Reusable Blood Pressure Cuff receive FDA 510(k) clearance?

Medline Reusable Blood Pressure Cuff received FDA 510(k) clearance on 2026-06-22, under 510(k) number K254287.

Who is the listed applicant for Medline Reusable Blood Pressure Cuff?

The FDA 510(k) record lists Medline Industries, LP as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Medline Reusable Blood Pressure Cuff?

The FDA product code for Medline Reusable Blood Pressure Cuff is DXQ.

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Fonte oficial

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