FDA 510(k)

Medline Integrated Arterial Catheter

N.º K: K210548 · 2022-05-17

Fecha de decisión2022-05-17

Código de productoDQX

Comité asesorCV

DecisiónSubstantially Equivalent

Resumen del dispositivo

Medline Integrated Arterial Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Centurion Medical Products. It received FDA 510(k) clearance on 2022-05-17 under 510(k) number K210548. The device is classified under product code DQX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Medline Integrated Arterial Catheter?

Medline Integrated Arterial Catheter is a medical device that received FDA 510(k) clearance on 2022-05-17. The listed applicant is Centurion Medical Products. The 510(k) number is K210548.

When did Medline Integrated Arterial Catheter receive FDA 510(k) clearance?

Medline Integrated Arterial Catheter received FDA 510(k) clearance on 2022-05-17, under 510(k) number K210548.

Who is the listed applicant for Medline Integrated Arterial Catheter?

The FDA 510(k) record lists Centurion Medical Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Medline Integrated Arterial Catheter?

The FDA product code for Medline Integrated Arterial Catheter is DQX.

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Fuente oficial

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