FDA 510(k)

Gastrointestinal Videoscope Olympus GIF-2T1500

Número K: K260824 · 2026-08-27

RequerenteOlympus Medical Systems Corporation

Data da decisão2026-08-27

Código do produtoFDS

Comité consultivoGU

DecisãoSubstantially Equivalent

Resumo do dispositivo

Gastrointestinal Videoscope Olympus GIF-2T1500 is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Medical Systems Corporation. It received FDA 510(k) clearance on 2026-08-27 under 510(k) number K260824. The device is classified under product code FDS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Gastrointestinal Videoscope Olympus GIF-2T1500?

Gastrointestinal Videoscope Olympus GIF-2T1500 is a medical device that received FDA 510(k) clearance on 2026-08-27. The listed applicant is Olympus Medical Systems Corporation. The 510(k) number is K260824.

When did Gastrointestinal Videoscope Olympus GIF-2T1500 receive FDA 510(k) clearance?

Gastrointestinal Videoscope Olympus GIF-2T1500 received FDA 510(k) clearance on 2026-08-27, under 510(k) number K260824.

Quem é o solicitante listado para o Gastrointestinal Videoscope Olympus GIF-2T1500?

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

What is the FDA product code for Gastrointestinal Videoscope Olympus GIF-2T1500?

The FDA product code for Gastrointestinal Videoscope Olympus GIF-2T1500 is FDS.

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Outros registros que listam Olympus Medical Systems Corporation como candidato(a)

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Fonte oficial

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