FDA 510(k)

Nam illumination probe with chopper

N.º K: K202670 · 2021-08-20

Fecha de decisión2021-08-20

Código de productoMPA

Comité asesorGU

DecisiónSubstantially Equivalent

Resumen del dispositivo

Nam illumination probe with chopper is the device name listed in this FDA 510(k) record. The listed applicant is Oculight , Ltd.. It received FDA 510(k) clearance on 2021-08-20 under 510(k) number K202670. The device is classified under product code MPA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Nam illumination probe with chopper?

Nam illumination probe with chopper is a medical device that received FDA 510(k) clearance on 2021-08-20. The listed applicant is Oculight , Ltd.. The 510(k) number is K202670.

When did Nam illumination probe with chopper receive FDA 510(k) clearance?

Nam illumination probe with chopper received FDA 510(k) clearance on 2021-08-20, under 510(k) number K202670.

Who is the listed applicant for Nam illumination probe with chopper?

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

What is the FDA product code for Nam illumination probe with chopper?

The FDA product code for Nam illumination probe with chopper is MPA.

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Fuente oficial

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