FDA 510(k)

Honda Walking Assist Device

N.º K: K181294 · 2018-12-14

Fecha de decisión2018-12-14

Código de productoPHL

Comité asesorPM

DecisiónSubstantially Equivalent

Resumen del dispositivo

Honda Walking Assist Device is the device name listed in this FDA 510(k) record. The listed applicant is Honda Motor Company, Ltd.. It received FDA 510(k) clearance on 2018-12-14 under 510(k) number K181294. The device is classified under product code PHL. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Honda Walking Assist Device?

Honda Walking Assist Device is a medical device that received FDA 510(k) clearance on 2018-12-14. The listed applicant is Honda Motor Company, Ltd.. The 510(k) number is K181294.

When did Honda Walking Assist Device receive FDA 510(k) clearance?

Honda Walking Assist Device received FDA 510(k) clearance on 2018-12-14, under 510(k) number K181294.

Who is the listed applicant for Honda Walking Assist Device?

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

What is the FDA product code for Honda Walking Assist Device?

The FDA product code for Honda Walking Assist Device is PHL.

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Fuente oficial

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