FDA 510(k)

Celesteion, PCA-9000A/3

Número K: K170490 · 2017-06-01

RequerenteToshibamedical Systems Corporation

Data da decisão2017-06-01

Código do produtoKPS

Comité consultivoRA

DecisãoSubstantially Equivalent

Resumo do dispositivo

Celesteion, PCA-9000A/3 is the device name listed in this FDA 510(k) record. The listed applicant is Toshibamedical Systems Corporation. It received FDA 510(k) clearance on 2017-06-01 under 510(k) number K170490. The device is classified under product code KPS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Celesteion, PCA-9000A/3?

Celesteion, PCA-9000A/3 is a medical device that received FDA 510(k) clearance on 2017-06-01. The listed applicant is Toshibamedical Systems Corporation. The 510(k) number is K170490.

When did Celesteion, PCA-9000A/3 receive FDA 510(k) clearance?

Celesteion, PCA-9000A/3 received FDA 510(k) clearance on 2017-06-01, under 510(k) number K170490.

Who is the listed applicant for Celesteion, PCA-9000A/3?

The FDA 510(k) record lists Toshibamedical Systems Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Celesteion, PCA-9000A/3?

The FDA product code for Celesteion, PCA-9000A/3 is KPS.

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