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FDA 510(k)

BOVIE ULTRASONIC SURGICAL ASPIRATOR, MODEL ME2000

K-Number: K880166 · 1988-02-18

ApplicantClinical Technology Corp.
Decision Date1988-02-18
Product CodeLFL
DecisionSubstantially Equivalent

Device Summary

BOVIE ULTRASONIC SURGICAL ASPIRATOR, MODEL ME2000 is the device name listed in this FDA 510(k) record. The listed applicant is Clinical Technology Corp.. It received FDA 510(k) clearance on 1988-02-18 under 510(k) number K880166. The device is classified under product code LFL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BOVIE ULTRASONIC SURGICAL ASPIRATOR, MODEL ME2000?

BOVIE ULTRASONIC SURGICAL ASPIRATOR, MODEL ME2000 is a medical device that received FDA 510(k) clearance on 1988-02-18. The listed applicant is Clinical Technology Corp.. The 510(k) number is K880166.

When did BOVIE ULTRASONIC SURGICAL ASPIRATOR, MODEL ME2000 receive FDA 510(k) clearance?

BOVIE ULTRASONIC SURGICAL ASPIRATOR, MODEL ME2000 received FDA 510(k) clearance on 1988-02-18, under 510(k) number K880166.

Who is the listed applicant for BOVIE ULTRASONIC SURGICAL ASPIRATOR, MODEL ME2000?

The FDA 510(k) record lists Clinical Technology Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BOVIE ULTRASONIC SURGICAL ASPIRATOR, MODEL ME2000?

The FDA product code for BOVIE ULTRASONIC SURGICAL ASPIRATOR, MODEL ME2000 is LFL.

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Other records listing Clinical Technology Corp. 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.

K925080TEK-LUBEK872867BIOSIGNK872705BOVIE 400-CT ELECTROSURGICAL GENERATOR (UNIT)K855138BOVIE ULTRASONIC SURGICAL SYSTEMK854231ELECTROSURGICAL CUTTING & COAGULATION DEVICE/ACCESK853507STERI-GRIP

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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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