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FDA 510(k)

LAPARO-THORACO VIDEOSCOPE XLTF-VAW

K-Number: K053382 · 2006-05-26

ApplicantOlympus Medical Systems Corporation
Decision Date2006-05-26
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LAPARO-THORACO VIDEOSCOPE XLTF-VAW 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 2006-05-26 under 510(k) number K053382. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAPARO-THORACO VIDEOSCOPE XLTF-VAW?

LAPARO-THORACO VIDEOSCOPE XLTF-VAW is a medical device that received FDA 510(k) clearance on 2006-05-26. The listed applicant is Olympus Medical Systems Corporation. The 510(k) number is K053382.

When did LAPARO-THORACO VIDEOSCOPE XLTF-VAW receive FDA 510(k) clearance?

LAPARO-THORACO VIDEOSCOPE XLTF-VAW received FDA 510(k) clearance on 2006-05-26, under 510(k) number K053382.

Who is the listed applicant for LAPARO-THORACO VIDEOSCOPE XLTF-VAW?

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 LAPARO-THORACO VIDEOSCOPE XLTF-VAW?

The FDA product code for LAPARO-THORACO VIDEOSCOPE XLTF-VAW is GCJ.

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Other records listing Olympus Medical Systems Corporation 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.

K260401EVIS EUS ULTRASOUND BRONCHOFIBERVIDEOSCOPE OLYMPUS BF-UCP190F (BF-UCP190F)K260824Gastrointestinal Videoscope Olympus GIF-2T1500K260856Disposable Distal Attachment D-201-13404K261183EVIS EUS Ultrasound Gastrointestinal Videoscope (Olympus GF-UE190)K261260HD Camera Head OLYMPUS CH-S200-08-LBK252050Disposable Biopsy Forceps FB-211D, FB-221D, FB-231D, FB-241D

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Related Devices (Code: GCJ)

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.

K262397CuratOR EX2742Eizo CorporationK260884UNIDRIVE Select SystemKarl Storz SE & CO. KGK260972OEV-271MUH LCD Monitor;OEV-321MUH LCD Monitor;OEV-431MUH LCD MonitorSony CorporationK261139VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103)Freyja Healthcare, LLCK253541EZ-Close™ (EZ Close Port Site Closing Device, EZ Close MAX Port Site Closing Device, EZ Close II Port Site Closing Device)Medical ImpactK261614LED LCD Monitor (OEV-271H)Lg Electronics.Inc

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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