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FDA 510(k)

CUSA(R) SYSTEM 200C/200T/200M/200H ULTRA ASPIRATOR

K-Number: K910696 · 1991-06-11

ApplicantValleylab, Inc.
Decision Date1991-06-11
Product CodeLFL
DecisionSubstantially Equivalent

Device Summary

CUSA(R) SYSTEM 200C/200T/200M/200H ULTRA ASPIRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1991-06-11 under 510(k) number K910696. The device is classified under product code LFL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CUSA(R) SYSTEM 200C/200T/200M/200H ULTRA ASPIRATOR?

CUSA(R) SYSTEM 200C/200T/200M/200H ULTRA ASPIRATOR is a medical device that received FDA 510(k) clearance on 1991-06-11. The listed applicant is Valleylab, Inc.. The 510(k) number is K910696.

When did CUSA(R) SYSTEM 200C/200T/200M/200H ULTRA ASPIRATOR receive FDA 510(k) clearance?

CUSA(R) SYSTEM 200C/200T/200M/200H ULTRA ASPIRATOR received FDA 510(k) clearance on 1991-06-11, under 510(k) number K910696.

Who is the listed applicant for CUSA(R) SYSTEM 200C/200T/200M/200H ULTRA ASPIRATOR?

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(R) SYSTEM 200C/200T/200M/200H ULTRA ASPIRATOR?

The FDA product code for CUSA(R) SYSTEM 200C/200T/200M/200H ULTRA ASPIRATOR 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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