FDA 510(k)

Quell

N.º K: K152954 · 2016-01-05

Fecha de decisión2016-01-05

Código de productoNUH

Comité asesorNE

DecisiónSubstantially Equivalent

Resumen del dispositivo

Quell is the device name listed in this FDA 510(k) record. The listed applicant is Neurometrix, Inc.. It received FDA 510(k) clearance on 2016-01-05 under 510(k) number K152954. The device is classified under product code NUH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Quell?

Quell is a medical device that received FDA 510(k) clearance on 2016-01-05. The listed applicant is Neurometrix, Inc.. The 510(k) number is K152954.

When did Quell receive FDA 510(k) clearance?

Quell received FDA 510(k) clearance on 2016-01-05, under 510(k) number K152954.

Who is the listed applicant for Quell?

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

What is the FDA product code for Quell?

The FDA product code for Quell is NUH.

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