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FDA 510(k)

OLYMPUS ULTRASONIC SURGICAL SYSTEM SONOSURG

K-Number: K050885 · 2005-06-03

ApplicantOlympus Medical Systems Corporation
Decision Date2005-06-03
Product CodeLFL
DecisionSubstantially Equivalent

Device Summary

OLYMPUS ULTRASONIC SURGICAL SYSTEM SONOSURG 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 2005-06-03 under 510(k) number K050885. The device is classified under product code LFL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OLYMPUS ULTRASONIC SURGICAL SYSTEM SONOSURG?

OLYMPUS ULTRASONIC SURGICAL SYSTEM SONOSURG is a medical device that received FDA 510(k) clearance on 2005-06-03. The listed applicant is Olympus Medical Systems Corporation. The 510(k) number is K050885.

When did OLYMPUS ULTRASONIC SURGICAL SYSTEM SONOSURG receive FDA 510(k) clearance?

OLYMPUS ULTRASONIC SURGICAL SYSTEM SONOSURG received FDA 510(k) clearance on 2005-06-03, under 510(k) number K050885.

Who is the listed applicant for OLYMPUS ULTRASONIC SURGICAL SYSTEM SONOSURG?

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 OLYMPUS ULTRASONIC SURGICAL SYSTEM SONOSURG?

The FDA product code for OLYMPUS ULTRASONIC SURGICAL SYSTEM SONOSURG is LFL.

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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

View all 86 devices →

Related Devices (Code: LFL)

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.

K261448neXus Ultrasonic Surgical Aspirator SystemMisonix, LLCK251162CUSA® Clarity Ultrasonic Surgical Aspirator SystemIntegra LifeSciences CorporationK242894SanAgile™ Ultrasonic Surgery Advanced Portable Controller (SA10); SanAgile™ Ultrasonic Surgery Advanced Dissector (SASD14); SanAgile™ Ultrasonic Surgery Advanced Dissector (SASD23); SanAgile™ Ultrasonic Surgery Advanced Dissector (SASD36); SanAgile™ Ultrasonic Surgery Advanced Dissector (SASD45)Shanghai Saints Sages Surgical Co., Ltd.K243930Sonopet iQ Ultrasonic Aspirator System (5500-050-000)Stryker InstrumentsK241700Tenex 2nd Generation SystemTrice Medical, Inc.K240493CUSA® Clarity Ultrasonic Surgical Aspirator SystemIntegra LifeSciences 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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