FDA 510(k)

Processor VP-7000, Light Source BL-7000X, Image Processing Unit EX-0

N.º K: K203717 · 2021-06-30

Fecha de decisión2021-06-30

Código de productoGCJ

Comité asesorGU

DecisiónSubstantially Equivalent

Resumen del dispositivo

Processor VP-7000, Light Source BL-7000X, Image Processing Unit EX-0 is the device name listed in this FDA 510(k) record. The listed applicant is Fujifilm Corporaton. It received FDA 510(k) clearance on 2021-06-30 under 510(k) number K203717. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Processor VP-7000, Light Source BL-7000X, Image Processing Unit EX-0?

Processor VP-7000, Light Source BL-7000X, Image Processing Unit EX-0 is a medical device that received FDA 510(k) clearance on 2021-06-30. The listed applicant is Fujifilm Corporaton. The 510(k) number is K203717.

When did Processor VP-7000, Light Source BL-7000X, Image Processing Unit EX-0 receive FDA 510(k) clearance?

Processor VP-7000, Light Source BL-7000X, Image Processing Unit EX-0 received FDA 510(k) clearance on 2021-06-30, under 510(k) number K203717.

Who is the listed applicant for Processor VP-7000, Light Source BL-7000X, Image Processing Unit EX-0?

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

What is the FDA product code for Processor VP-7000, Light Source BL-7000X, Image Processing Unit EX-0?

The FDA product code for Processor VP-7000, Light Source BL-7000X, Image Processing Unit EX-0 is GCJ.

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Otros registros que enlistan a Fujifilm Corporaton como solicitante

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Fuente oficial

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