FDA 510(k)

Pluski Safe 1 Safety IV Catheter

N.º K: K210037 · 2022-03-25

Fecha de decisión2022-03-25

Código de productoFOZ

Comité asesorHO

DecisiónSubstantially Equivalent

Resumen del dispositivo

Pluski Safe 1 Safety IV Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Mediplus (India) Limited. It received FDA 510(k) clearance on 2022-03-25 under 510(k) number K210037. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Pluski Safe 1 Safety IV Catheter?

Pluski Safe 1 Safety IV Catheter is a medical device that received FDA 510(k) clearance on 2022-03-25. The listed applicant is Mediplus (India) Limited. The 510(k) number is K210037.

When did Pluski Safe 1 Safety IV Catheter receive FDA 510(k) clearance?

Pluski Safe 1 Safety IV Catheter received FDA 510(k) clearance on 2022-03-25, under 510(k) number K210037.

Who is the listed applicant for Pluski Safe 1 Safety IV Catheter?

The FDA 510(k) record lists Mediplus (India) Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Pluski Safe 1 Safety IV Catheter?

The FDA product code for Pluski Safe 1 Safety IV Catheter is FOZ.

Ensayos clínicos relacionados

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Fuente oficial

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