FDA 510(k)

FilmArray Pneumonia/Pneumoniaplus Control

Número K: K190222 · 2019-05-03

RequerenteMaine Molecular Quality Controls, Inc.

Data da decisão2019-05-03

Código do produtoPMN

Comité consultivoMI

DecisãoSubstantially Equivalent

Resumo do dispositivo

FilmArray Pneumonia/Pneumoniaplus Control is the device name listed in this FDA 510(k) record. The listed applicant is Maine Molecular Quality Controls, Inc.. It received FDA 510(k) clearance on 2019-05-03 under 510(k) number K190222. The device is classified under product code PMN. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the FilmArray Pneumonia/Pneumoniaplus Control?

FilmArray Pneumonia/Pneumoniaplus Control is a medical device that received FDA 510(k) clearance on 2019-05-03. The listed applicant is Maine Molecular Quality Controls, Inc.. The 510(k) number is K190222.

When did FilmArray Pneumonia/Pneumoniaplus Control receive FDA 510(k) clearance?

FilmArray Pneumonia/Pneumoniaplus Control received FDA 510(k) clearance on 2019-05-03, under 510(k) number K190222.

Who is the listed applicant for FilmArray Pneumonia/Pneumoniaplus Control?

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

What is the FDA product code for FilmArray Pneumonia/Pneumoniaplus Control?

The FDA product code for FilmArray Pneumonia/Pneumoniaplus Control is PMN.

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Fonte oficial

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