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FDA 510(k)

OLYMPUS XGIF-N200H GASTROINTESTINAL VIDEOSCOPE

K-Number: K001766 · 2000-09-08

ApplicantOlympus Optical Co., Ltd.
Decision Date2000-09-08
Product CodeFDS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

OLYMPUS XGIF-N200H GASTROINTESTINAL VIDEOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Optical Co., Ltd.. It received FDA 510(k) clearance on 2000-09-08 under 510(k) number K001766. 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 OLYMPUS XGIF-N200H GASTROINTESTINAL VIDEOSCOPE?

OLYMPUS XGIF-N200H GASTROINTESTINAL VIDEOSCOPE is a medical device that received FDA 510(k) clearance on 2000-09-08. The listed applicant is Olympus Optical Co., Ltd.. The 510(k) number is K001766.

When did OLYMPUS XGIF-N200H GASTROINTESTINAL VIDEOSCOPE receive FDA 510(k) clearance?

OLYMPUS XGIF-N200H GASTROINTESTINAL VIDEOSCOPE received FDA 510(k) clearance on 2000-09-08, under 510(k) number K001766.

Who is the listed applicant for OLYMPUS XGIF-N200H GASTROINTESTINAL VIDEOSCOPE?

The FDA 510(k) record lists Olympus Optical Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OLYMPUS XGIF-N200H GASTROINTESTINAL VIDEOSCOPE?

The FDA product code for OLYMPUS XGIF-N200H GASTROINTESTINAL VIDEOSCOPE is FDS.

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Other records listing Olympus Optical Co., Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K033225EVIS EXERA BRONCHOFIBERVIDEOSCOPE OLYMPUS BF TYPE XP160F, ITS ACCESSORIES AND ANCILLARY EQUIPMENTK031305OLYMPUS ULTRASONIC SURGICAL SYSTEMK031648VISERA RHINO-LARYNGOVIDEOSCOPE OLYMPUS ENF TYPE VK032092OLYMPUS XCYF-TP3 CYSTOFIBERSCOPE/NEPHROFIBERSCOPEK031347ULTRASONIC GASTROVIDEOSCOPE, TYPE UC160P-AT8 AND UCT160-AT8K024138HEAT SCISSORS GENERATOR SET AND HEAT SCISSORS HANDPIECE

View all 22 devices →

Related Devices (Code: FDS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261400Ambu® aScope™ Gastro; Ambu® aScope™ Gastro LargeAmbu A/SK260856Disposable Distal Attachment D-201-13404Olympus Medical Systems CorporationK260824Gastrointestinal Videoscope Olympus GIF-2T1500Olympus Medical Systems CorporationK253702Intuitive Endoluminal Gastrointestinal System (IG1000)Intuitive Surgical, Inc.K260573EvoEndo Single-Use Endoscopy SystemEvoEndo, Inc.K250550FUJIFILM Endoscope Model EG-S100XT and VS-1000 Display UnitFujifilm Corporation

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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