FDA 510(k)

Ingenuity TF

N.º K: K172406 · 2017-10-06

SolicitantePhilips Medical Systems (Cleveland), Inc.

Fecha de decisión2017-10-06

Código de productoKPS

Comité asesorRA

DecisiónSubstantially Equivalent

Resumen del dispositivo

Ingenuity TF is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems (Cleveland), Inc.. It received FDA 510(k) clearance on 2017-10-06 under 510(k) number K172406. The device is classified under product code KPS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Ingenuity TF?

Ingenuity TF is a medical device that received FDA 510(k) clearance on 2017-10-06. The listed applicant is Philips Medical Systems (Cleveland), Inc.. The 510(k) number is K172406.

When did Ingenuity TF receive FDA 510(k) clearance?

Ingenuity TF received FDA 510(k) clearance on 2017-10-06, under 510(k) number K172406.

Who is the listed applicant for Ingenuity TF?

The FDA 510(k) record lists Philips Medical Systems (Cleveland), Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Ingenuity TF?

The FDA product code for Ingenuity TF is KPS.

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Otros registros que enlistan a Philips Medical Systems (Cleveland), Inc. como solicitante

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Fuente oficial

Ver en la base de datos de la FDA →

Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.