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FDA 510(k)

XSIF-1TQ140A SMALL INTESTINAL VIDEOSCOPE

K-Number: K031256 · 2003-07-23

ApplicantOlympus Opto-Electronics Co., Ltd.
Decision Date2003-07-23
Product CodeFDA
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

XSIF-1TQ140A SMALL INTESTINAL VIDEOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Opto-Electronics Co., Ltd.. It received FDA 510(k) clearance on 2003-07-23 under 510(k) number K031256. The device is classified under product code FDA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the XSIF-1TQ140A SMALL INTESTINAL VIDEOSCOPE?

XSIF-1TQ140A SMALL INTESTINAL VIDEOSCOPE is a medical device that received FDA 510(k) clearance on 2003-07-23. The listed applicant is Olympus Opto-Electronics Co., Ltd.. The 510(k) number is K031256.

When did XSIF-1TQ140A SMALL INTESTINAL VIDEOSCOPE receive FDA 510(k) clearance?

XSIF-1TQ140A SMALL INTESTINAL VIDEOSCOPE received FDA 510(k) clearance on 2003-07-23, under 510(k) number K031256.

Who is the listed applicant for XSIF-1TQ140A SMALL INTESTINAL VIDEOSCOPE?

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

What is the FDA product code for XSIF-1TQ140A SMALL INTESTINAL VIDEOSCOPE?

The FDA product code for XSIF-1TQ140A SMALL INTESTINAL VIDEOSCOPE is FDA.

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Other records listing Olympus Opto-Electronics 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.

K032177GASTROINTESTINAL VIDEOSCOPE XGIF-Q14OM, XGIF-2T140M COLONOVIDEOSCOPE XCF-Q14ML/I, XPCF-160AML/I

Related Devices (Code: FDA)

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.

K260314Ancora-SBAspero Medical, Inc.K251204FUJIFILM Stiffening Wire Device (SW-2000)FUJIFILM Healthcare Americas CorporationK233321Double Balloon Endoscope EN-840T, Over-tube TS-1214CFUJIFILM Healthcare Americas CorporationK231323Ancora-SBAspero Medical, Inc.K223295Endoscope Model EN-580T, Over-tube TS-1314B, Balloon BS-4, Tube Kit TY-500DFujifilm CorporatonK213195Balloon BS-3Fujifilm Corporation

Official Source

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

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