FDA 510(k)

Master-Frank N95 Particulate Respirator

N.º K: K172963 · 2018-04-04

SolicitanteMaster & Frank Enterprise Co., Ltd.

Fecha de decisión2018-04-04

Código de productoMSH

Comité asesorSU

DecisiónSubstantially Equivalent

Resumen del dispositivo

Master-Frank N95 Particulate Respirator is the device name listed in this FDA 510(k) record. The listed applicant is Master & Frank Enterprise Co., Ltd.. It received FDA 510(k) clearance on 2018-04-04 under 510(k) number K172963. The device is classified under product code MSH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Master-Frank N95 Particulate Respirator?

Master-Frank N95 Particulate Respirator is a medical device that received FDA 510(k) clearance on 2018-04-04. The listed applicant is Master & Frank Enterprise Co., Ltd.. The 510(k) number is K172963.

When did Master-Frank N95 Particulate Respirator receive FDA 510(k) clearance?

Master-Frank N95 Particulate Respirator received FDA 510(k) clearance on 2018-04-04, under 510(k) number K172963.

Who is the listed applicant for Master-Frank N95 Particulate Respirator?

The FDA 510(k) record lists Master & Frank Enterprise Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Master-Frank N95 Particulate Respirator?

The FDA product code for Master-Frank N95 Particulate Respirator is MSH.

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Dispositivos relacionados (Código: MSH)

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Fuente oficial

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