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FDA 510(k)

CUSA SYSTEM 200C/T ULTRASONIC ASPIRATOR & ACCESS.

K-Number: K931902 · 1994-09-16

ApplicantValleylab, Inc.
Decision Date1994-09-16
Product CodeLFL
DecisionSubstantially Equivalent

Device Summary

CUSA SYSTEM 200C/T ULTRASONIC ASPIRATOR & ACCESS. is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1994-09-16 under 510(k) number K931902. The device is classified under product code LFL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CUSA SYSTEM 200C/T ULTRASONIC ASPIRATOR & ACCESS.?

CUSA SYSTEM 200C/T ULTRASONIC ASPIRATOR & ACCESS. is a medical device that received FDA 510(k) clearance on 1994-09-16. The listed applicant is Valleylab, Inc.. The 510(k) number is K931902.

When did CUSA SYSTEM 200C/T ULTRASONIC ASPIRATOR & ACCESS. receive FDA 510(k) clearance?

CUSA SYSTEM 200C/T ULTRASONIC ASPIRATOR & ACCESS. received FDA 510(k) clearance on 1994-09-16, under 510(k) number K931902.

Who is the listed applicant for CUSA SYSTEM 200C/T ULTRASONIC ASPIRATOR & ACCESS.?

The FDA 510(k) record lists Valleylab, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CUSA SYSTEM 200C/T ULTRASONIC ASPIRATOR & ACCESS.?

The FDA product code for CUSA SYSTEM 200C/T ULTRASONIC ASPIRATOR & ACCESS. is LFL.

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Other records listing Valleylab, Inc. 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.

K031011LIGASURE 5MM LAPAROSCOPIC SEALER-DIVIDER, MODEL LS1500K010010VALLEYLAB LIGASURE PRECISE INSTRUMENT VESSEL SEALING SYSTEM-MODEL # LS1200 & SLIGAURE GENERATORK010013LIGASURE LAPAROSCOPIC SEALER DIVIDER MODEL LS1100K994428E7512 PREMIE REM POLYHESIVE II PATIENT RETURN ELECTRODEK983743BISURE LAPAROSCOPIC BIPOLAR FORCEPSK981916LIGASURE VESSEL SEALING SYSTEM

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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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