FDA 510(k)

Revive Reusable Bladder Support

N.º K: K183468 · 2019-01-25

Fecha de decisión2019-01-25

Código de productoHHW

Comité asesorOB

DecisiónSubstantially Equivalent

Resumen del dispositivo

Revive Reusable Bladder Support is the device name listed in this FDA 510(k) record. The listed applicant is Rinovum Subsidiary 2, LLC. It received FDA 510(k) clearance on 2019-01-25 under 510(k) number K183468. The device is classified under product code HHW. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Revive Reusable Bladder Support?

Revive Reusable Bladder Support is a medical device that received FDA 510(k) clearance on 2019-01-25. The listed applicant is Rinovum Subsidiary 2, LLC. The 510(k) number is K183468.

When did Revive Reusable Bladder Support receive FDA 510(k) clearance?

Revive Reusable Bladder Support received FDA 510(k) clearance on 2019-01-25, under 510(k) number K183468.

Who is the listed applicant for Revive Reusable Bladder Support?

The FDA 510(k) record lists Rinovum Subsidiary 2, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Revive Reusable Bladder Support?

The FDA product code for Revive Reusable Bladder Support is HHW.

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Dispositivos relacionados (Código: HHW)

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Fuente oficial

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