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FDA 510(k)

Armory Motion

N.º K: K213097 · 2022-06-10

SolicitantePain Management Technologies, Inc.
Fecha de decisión2022-06-10
Código de productoILO
Comité asesorPM
DecisiónSubstantially Equivalent

Resumen del dispositivo

Armory Motion is the device name listed in this FDA 510(k) record. The listed applicant is Pain Management Technologies, Inc.. It received FDA 510(k) clearance on 2022-06-10 under 510(k) number K213097. The device is classified under product code ILO. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Armory Motion?

Armory Motion is a medical device that received FDA 510(k) clearance on 2022-06-10. The listed applicant is Pain Management Technologies, Inc.. The 510(k) number is K213097.

When did Armory Motion receive FDA 510(k) clearance?

Armory Motion received FDA 510(k) clearance on 2022-06-10, under 510(k) number K213097.

Who is the listed applicant for Armory Motion?

The FDA 510(k) record lists Pain Management Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Armory Motion?

The FDA product code for Armory Motion is ILO.

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Fuente oficial

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