FDA 510(k)

Seer Home

N.º K: K212788 · 2022-06-16

Fecha de decisión2022-06-16

Código de productoGWQ

Comité asesorNE

DecisiónSubstantially Equivalent

Resumen del dispositivo

Seer Home is the device name listed in this FDA 510(k) record. The listed applicant is Seer Medical Pty, Ltd.. It received FDA 510(k) clearance on 2022-06-16 under 510(k) number K212788. The device is classified under product code GWQ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Seer Home?

Seer Home is a medical device that received FDA 510(k) clearance on 2022-06-16. The listed applicant is Seer Medical Pty, Ltd.. The 510(k) number is K212788.

When did Seer Home receive FDA 510(k) clearance?

Seer Home received FDA 510(k) clearance on 2022-06-16, under 510(k) number K212788.

Who is the listed applicant for Seer Home?

The FDA 510(k) record lists Seer Medical Pty, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Seer Home?

The FDA product code for Seer Home is GWQ.

Dispositivos relacionados (Código: GWQ)

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Fuente oficial

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