FDA 510(k)

Impress Angiographic Catheter

N.º K: K233268 · 2024-05-22

Fecha de decisión2024-05-22

Código de productoDQO

Comité asesorCV

DecisiónSubstantially Equivalent

Resumen del dispositivo

Impress Angiographic Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Merit Medical Systems, Inc.. It received FDA 510(k) clearance on 2024-05-22 under 510(k) number K233268. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Impress Angiographic Catheter?

Impress Angiographic Catheter is a medical device that received FDA 510(k) clearance on 2024-05-22. The listed applicant is Merit Medical Systems, Inc.. The 510(k) number is K233268.

When did Impress Angiographic Catheter receive FDA 510(k) clearance?

Impress Angiographic Catheter received FDA 510(k) clearance on 2024-05-22, under 510(k) number K233268.

Who is the listed applicant for Impress Angiographic Catheter?

The FDA 510(k) record lists Merit Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Impress Angiographic Catheter?

The FDA product code for Impress Angiographic Catheter is DQO.

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Fuente oficial

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