FDA 510(k)

CP Relief Wand-OTC

N.º K: K162630 · 2016-12-20

SolicitanteMid-America Medical Innovations, LLC

Fecha de decisión2016-12-20

Código de productoNUH

Comité asesorNE

DecisiónSubstantially Equivalent

Resumen del dispositivo

CP Relief Wand-OTC is the device name listed in this FDA 510(k) record. The listed applicant is Mid-America Medical Innovations, LLC. It received FDA 510(k) clearance on 2016-12-20 under 510(k) number K162630. 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 CP Relief Wand-OTC?

CP Relief Wand-OTC is a medical device that received FDA 510(k) clearance on 2016-12-20. The listed applicant is Mid-America Medical Innovations, LLC. The 510(k) number is K162630.

When did CP Relief Wand-OTC receive FDA 510(k) clearance?

CP Relief Wand-OTC received FDA 510(k) clearance on 2016-12-20, under 510(k) number K162630.

Who is the listed applicant for CP Relief Wand-OTC?

The FDA 510(k) record lists Mid-America Medical Innovations, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CP Relief Wand-OTC?

The FDA product code for CP Relief Wand-OTC is NUH.

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Fuente oficial

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