FDA 510(k)

TELIGEN System Peripheral Motor Nerve Stimulation Indications

N.º K: K223438 · 2023-02-10

Fecha de decisión2023-02-10

Código de productoPDQ

Comité asesorEN

DecisiónSubstantially Equivalent

Resumen del dispositivo

TELIGEN System Peripheral Motor Nerve Stimulation Indications is the device name listed in this FDA 510(k) record. The listed applicant is Medos International SARL. It received FDA 510(k) clearance on 2023-02-10 under 510(k) number K223438. The device is classified under product code PDQ. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the TELIGEN System Peripheral Motor Nerve Stimulation Indications?

TELIGEN System Peripheral Motor Nerve Stimulation Indications is a medical device that received FDA 510(k) clearance on 2023-02-10. The listed applicant is Medos International SARL. The 510(k) number is K223438.

When did TELIGEN System Peripheral Motor Nerve Stimulation Indications receive FDA 510(k) clearance?

TELIGEN System Peripheral Motor Nerve Stimulation Indications received FDA 510(k) clearance on 2023-02-10, under 510(k) number K223438.

Who is the listed applicant for TELIGEN System Peripheral Motor Nerve Stimulation Indications?

The FDA 510(k) record lists Medos International SARL as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TELIGEN System Peripheral Motor Nerve Stimulation Indications?

The FDA product code for TELIGEN System Peripheral Motor Nerve Stimulation Indications is PDQ.

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Fuente oficial

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