FDA 510(k)

LOGIC 4K CAMERA CONTROLLER, LOGIC 4K CAMERA HEAD

N.º K: K180583 · 2018-06-28

SolicitanteRichard Wolf Medical Instruments Corporation

Fecha de decisión2018-06-28

Código de productoFET

Comité asesorGU

DecisiónSubstantially Equivalent

Resumen del dispositivo

LOGIC 4K CAMERA CONTROLLER, LOGIC 4K CAMERA HEAD is the device name listed in this FDA 510(k) record. The listed applicant is Richard Wolf Medical Instruments Corporation. It received FDA 510(k) clearance on 2018-06-28 under 510(k) number K180583. The device is classified under product code FET. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the LOGIC 4K CAMERA CONTROLLER, LOGIC 4K CAMERA HEAD?

LOGIC 4K CAMERA CONTROLLER, LOGIC 4K CAMERA HEAD is a medical device that received FDA 510(k) clearance on 2018-06-28. The listed applicant is Richard Wolf Medical Instruments Corporation. The 510(k) number is K180583.

When did LOGIC 4K CAMERA CONTROLLER, LOGIC 4K CAMERA HEAD receive FDA 510(k) clearance?

LOGIC 4K CAMERA CONTROLLER, LOGIC 4K CAMERA HEAD received FDA 510(k) clearance on 2018-06-28, under 510(k) number K180583.

Who is the listed applicant for LOGIC 4K CAMERA CONTROLLER, LOGIC 4K CAMERA HEAD?

The FDA 510(k) record lists Richard Wolf Medical Instruments Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LOGIC 4K CAMERA CONTROLLER, LOGIC 4K CAMERA HEAD?

The FDA product code for LOGIC 4K CAMERA CONTROLLER, LOGIC 4K CAMERA HEAD is FET.

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Fuente oficial

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