FDA 510(k)

Flex-MI

N.º K: K221958 · 2022-10-21

Fecha de decisión2022-10-21

Código de productoIPF

Comité asesorPM

DecisiónSubstantially Equivalent

Resumen del dispositivo

Flex-MI is the device name listed in this FDA 510(k) record. The listed applicant is Emsi, Inc.. It received FDA 510(k) clearance on 2022-10-21 under 510(k) number K221958. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Flex-MI?

Flex-MI is a medical device that received FDA 510(k) clearance on 2022-10-21. The listed applicant is Emsi, Inc.. The 510(k) number is K221958.

When did Flex-MI receive FDA 510(k) clearance?

Flex-MI received FDA 510(k) clearance on 2022-10-21, under 510(k) number K221958.

Who is the listed applicant for Flex-MI?

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

What is the FDA product code for Flex-MI?

The FDA product code for Flex-MI is IPF.

Dispositivos relacionados (Código: IPF)

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Fuente oficial

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