FDA 510(k)

YandR System, VoluDerm Handpiece, VoluDerm Tips

N.º K: K220124 · 2022-02-17

Fecha de decisión2022-02-17

Código de productoGEI

Comité asesorSU

DecisiónSubstantially Equivalent

Resumen del dispositivo

YandR System, VoluDerm Handpiece, VoluDerm Tips is the device name listed in this FDA 510(k) record. The listed applicant is Pollogen, Ltd.. It received FDA 510(k) clearance on 2022-02-17 under 510(k) number K220124. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the YandR System, VoluDerm Handpiece, VoluDerm Tips?

YandR System, VoluDerm Handpiece, VoluDerm Tips is a medical device that received FDA 510(k) clearance on 2022-02-17. The listed applicant is Pollogen, Ltd.. The 510(k) number is K220124.

When did YandR System, VoluDerm Handpiece, VoluDerm Tips receive FDA 510(k) clearance?

YandR System, VoluDerm Handpiece, VoluDerm Tips received FDA 510(k) clearance on 2022-02-17, under 510(k) number K220124.

Who is the listed applicant for YandR System, VoluDerm Handpiece, VoluDerm Tips?

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

What is the FDA product code for YandR System, VoluDerm Handpiece, VoluDerm Tips?

The FDA product code for YandR System, VoluDerm Handpiece, VoluDerm Tips is GEI.

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Fuente oficial

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