FDA 510(k)

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

K-번호: K250550 · 2026-02-17

결정일2026-02-17

제품 코드FDS

자문 위원회GU

결정Substantially Equivalent

기기 요약

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

자주 묻는 질문

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. The listed applicant is Fujifilm Corporation. The 510(k) number is K250550.

When did FUJIFILM Endoscope Model EG-S100XT and VS-1000 Display Unit receive FDA 510(k) clearance?

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

Who is the listed applicant for FUJIFILM Endoscope Model EG-S100XT and VS-1000 Display Unit?

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

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.

Fujifilm Corporation를 신청인으로 등재한 기타 기록

K261229SCENARIA View Phase 6.0 K261283APERTO Lucent MRI System K253836FCT iStream Phase 2 K261170BA-004CC K260567EW10-EC02 Endoscopy Support Program K261880FUJIFILM Processor EP-8000;Balloon Controller PB-30;Endoscopy Support Program EW10-VM01

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