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FDA 510(k)

PowerPICC Provena Catheters

N.º K: K162443 · 2016-10-25

SolicitanteC.R. Bard, Inc.
Fecha de decisión2016-10-25
Código de productoLJS
Comité asesorHO
DecisiónSubstantially Equivalent

Resumen del dispositivo

PowerPICC Provena Catheters is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 2016-10-25 under 510(k) number K162443. The device is classified under product code LJS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the PowerPICC Provena Catheters?

PowerPICC Provena Catheters is a medical device that received FDA 510(k) clearance on 2016-10-25. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K162443.

When did PowerPICC Provena Catheters receive FDA 510(k) clearance?

PowerPICC Provena Catheters received FDA 510(k) clearance on 2016-10-25, under 510(k) number K162443.

Who is the listed applicant for PowerPICC Provena Catheters?

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

What is the FDA product code for PowerPICC Provena Catheters?

The FDA product code for PowerPICC Provena Catheters is LJS.

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Dispositivos relacionados (Código: LJS)

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Fuente oficial

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