FDA 510(k)

PureWay 1.4 Quart Sharps Collector

N.º K: K231484 · 2023-09-14

Fecha de decisión2023-09-14

Código de productoMMK

Comité asesorHO

DecisiónSubstantially Equivalent

Resumen del dispositivo

PureWay 1.4 Quart Sharps Collector is the device name listed in this FDA 510(k) record. The listed applicant is Pureway Compliance, Inc.. It received FDA 510(k) clearance on 2023-09-14 under 510(k) number K231484. The device is classified under product code MMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the PureWay 1.4 Quart Sharps Collector?

PureWay 1.4 Quart Sharps Collector is a medical device that received FDA 510(k) clearance on 2023-09-14. The listed applicant is Pureway Compliance, Inc.. The 510(k) number is K231484.

When did PureWay 1.4 Quart Sharps Collector receive FDA 510(k) clearance?

PureWay 1.4 Quart Sharps Collector received FDA 510(k) clearance on 2023-09-14, under 510(k) number K231484.

Who is the listed applicant for PureWay 1.4 Quart Sharps Collector?

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

What is the FDA product code for PureWay 1.4 Quart Sharps Collector?

The FDA product code for PureWay 1.4 Quart Sharps Collector is MMK.

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Otros registros que enlistan a Pureway Compliance, Inc. como solicitante

K251874PureWay Sharps Container 1-Gal, 2-Gal, 3-Gal (800011 800012, 800013)

Dispositivos relacionados (Código: MMK)

Fuente oficial

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