FDA 510(k)

Recovery Cone Removal System

N.º K: K152136 · 2016-02-18

Fecha de decisión2016-02-18

Código de productoMMX

Comité asesorCV

DecisiónSubstantially Equivalent

Resumen del dispositivo

Recovery Cone Removal System 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 2016-02-18 under 510(k) number K152136. The device is classified under product code MMX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Recovery Cone Removal System?

Recovery Cone Removal System is a medical device that received FDA 510(k) clearance on 2016-02-18. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K152136.

When did Recovery Cone Removal System receive FDA 510(k) clearance?

Recovery Cone Removal System received FDA 510(k) clearance on 2016-02-18, under 510(k) number K152136.

Who is the listed applicant for Recovery Cone Removal System?

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 Recovery Cone Removal System?

The FDA product code for Recovery Cone Removal System is MMX.

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Fuente oficial

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