FDA 510(k)

Progreat Lambda

N.º K: K211078 · 2021-12-21

SolicitanteTerumo Clinical Supply Co., Ltd.

Fecha de decisión2021-12-21

Código de productoDQO

Comité asesorCV

DecisiónSubstantially Equivalent

Resumen del dispositivo

Progreat Lambda is the device name listed in this FDA 510(k) record. The listed applicant is Terumo Clinical Supply Co., Ltd.. It received FDA 510(k) clearance on 2021-12-21 under 510(k) number K211078. The device is classified under product code DQO. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Progreat Lambda?

Progreat Lambda is a medical device that received FDA 510(k) clearance on 2021-12-21. The listed applicant is Terumo Clinical Supply Co., Ltd.. The 510(k) number is K211078.

When did Progreat Lambda receive FDA 510(k) clearance?

Progreat Lambda received FDA 510(k) clearance on 2021-12-21, under 510(k) number K211078.

Who is the listed applicant for Progreat Lambda?

The FDA 510(k) record lists Terumo Clinical Supply Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Progreat Lambda?

The FDA product code for Progreat Lambda is DQO.

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Fuente oficial

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