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FDA 510(k)

Ultrasonic Surgical System

K-Number: K210567 · 2022-09-30

ApplicantMiconvey Technologies Co., Ltd.
Decision Date2022-09-30
Product CodeLFL
DecisionSubstantially Equivalent

Device Summary

Ultrasonic Surgical System is the device name listed in this FDA 510(k) record. The listed applicant is Miconvey Technologies Co., Ltd.. It received FDA 510(k) clearance on 2022-09-30 under 510(k) number K210567. The device is classified under product code LFL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Ultrasonic Surgical System?

Ultrasonic Surgical System is a medical device that received FDA 510(k) clearance on 2022-09-30. The listed applicant is Miconvey Technologies Co., Ltd.. The 510(k) number is K210567.

When did Ultrasonic Surgical System receive FDA 510(k) clearance?

Ultrasonic Surgical System received FDA 510(k) clearance on 2022-09-30, under 510(k) number K210567.

Who is the listed applicant for Ultrasonic Surgical System?

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

What is the FDA product code for Ultrasonic Surgical System?

The FDA product code for Ultrasonic Surgical System is LFL.

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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