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FDA 510(k)

FUJIFILM Endoscope Model EG-S100XT and VS-1000 Display Unit

K-Number: K250550 · 2026-02-17

ApplicantFujifilm Corporation
Decision Date2026-02-17
Product CodeFDS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FUJIFILM Endoscope Model EG-S100XT and VS-1000 Display Unit is a medical device manufactured by Fujifilm Corporation. It received FDA 510(k) clearance on 2026-02-17 under approval number K250550. The device is classified under product code FDS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FUJIFILM Endoscope Model EG-S100XT and VS-1000 Display Unit?

FUJIFILM Endoscope Model EG-S100XT and VS-1000 Display Unit is a medical device that received FDA 510(k) clearance on 2026-02-17. It is manufactured by Fujifilm Corporation. The 510(k) number is K250550.

When was FUJIFILM Endoscope Model EG-S100XT and VS-1000 Display Unit approved by the FDA?

FUJIFILM Endoscope Model EG-S100XT and VS-1000 Display Unit received FDA 510(k) clearance on 2026-02-17, under approval number K250550.

What company makes FUJIFILM Endoscope Model EG-S100XT and VS-1000 Display Unit?

FUJIFILM Endoscope Model EG-S100XT and VS-1000 Display Unit is manufactured by Fujifilm Corporation.

What is the FDA product code for FUJIFILM Endoscope Model EG-S100XT and VS-1000 Display Unit?

The FDA product code for FUJIFILM Endoscope Model EG-S100XT and VS-1000 Display Unit is FDS.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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