FDA 510(k)

Evis Exera III Duodenovideoscope Olympus TJF-Q190V

Número K: K220587 · 2022-05-11

Data da decisão2022-05-11

Código do produtoFDT

Comité consultivoGU

DecisãoSubstantially Equivalent

Resumo do dispositivo

Evis Exera III Duodenovideoscope Olympus TJF-Q190V is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Medical Systems Corp.. It received FDA 510(k) clearance on 2022-05-11 under 510(k) number K220587. The device is classified under product code FDT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Evis Exera III Duodenovideoscope Olympus TJF-Q190V?

Evis Exera III Duodenovideoscope Olympus TJF-Q190V is a medical device that received FDA 510(k) clearance on 2022-05-11. The listed applicant is Olympus Medical Systems Corp.. The 510(k) number is K220587.

When did Evis Exera III Duodenovideoscope Olympus TJF-Q190V receive FDA 510(k) clearance?

Evis Exera III Duodenovideoscope Olympus TJF-Q190V received FDA 510(k) clearance on 2022-05-11, under 510(k) number K220587.

Who is the listed applicant for Evis Exera III Duodenovideoscope Olympus TJF-Q190V?

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

What is the FDA product code for Evis Exera III Duodenovideoscope Olympus TJF-Q190V?

The FDA product code for Evis Exera III Duodenovideoscope Olympus TJF-Q190V is FDT.

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