FDA 510(k)

CP Relief Wand Rx - TENS/NMES

N.º K: K252236 · 2025-08-15

Fecha de decisión2025-08-15

Código de productoGZJ

Comité asesorNE

DecisiónSubstantially Equivalent

Resumen del dispositivo

CP Relief Wand Rx - TENS/NMES is the device name listed in this FDA 510(k) record. The listed applicant is N & C Holdings, LLC. It received FDA 510(k) clearance on 2025-08-15 under 510(k) number K252236. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the CP Relief Wand Rx - TENS/NMES?

CP Relief Wand Rx - TENS/NMES is a medical device that received FDA 510(k) clearance on 2025-08-15. The listed applicant is N & C Holdings, LLC. The 510(k) number is K252236.

When did CP Relief Wand Rx - TENS/NMES receive FDA 510(k) clearance?

CP Relief Wand Rx - TENS/NMES received FDA 510(k) clearance on 2025-08-15, under 510(k) number K252236.

Who is the listed applicant for CP Relief Wand Rx - TENS/NMES?

The FDA 510(k) record lists N & C Holdings, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CP Relief Wand Rx - TENS/NMES?

The FDA product code for CP Relief Wand Rx - TENS/NMES is GZJ.

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Fuente oficial

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