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FDA 510(k)

CUSA SYSTEM 200C,T & M ULTRASONIC SURGICAL ASPIRA.

K-Number: K884412 · 1988-12-02

ApplicantValleylab, Inc.
Decision Date1988-12-02
Product CodeLBK
DecisionSubstantially Equivalent

Device Summary

CUSA SYSTEM 200C,T & M ULTRASONIC SURGICAL ASPIRA. is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1988-12-02 under 510(k) number K884412. The device is classified under product code LBK. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CUSA SYSTEM 200C,T & M ULTRASONIC SURGICAL ASPIRA.?

CUSA SYSTEM 200C,T & M ULTRASONIC SURGICAL ASPIRA. is a medical device that received FDA 510(k) clearance on 1988-12-02. The listed applicant is Valleylab, Inc.. The 510(k) number is K884412.

When did CUSA SYSTEM 200C,T & M ULTRASONIC SURGICAL ASPIRA. receive FDA 510(k) clearance?

CUSA SYSTEM 200C,T & M ULTRASONIC SURGICAL ASPIRA. received FDA 510(k) clearance on 1988-12-02, under 510(k) number K884412.

Who is the listed applicant for CUSA SYSTEM 200C,T & M ULTRASONIC SURGICAL ASPIRA.?

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 & M ULTRASONIC SURGICAL ASPIRA.?

The FDA product code for CUSA SYSTEM 200C,T & M ULTRASONIC SURGICAL ASPIRA. is LBK.

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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: LBK)

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.

K972612DISSECTRON PORTABLE UNITSatelecK962952OLYMPUS ULTRASONIC SURGICAL SYSTEM (USU)Olympus Optical, Co.K884413CUSA SYSTEM 200H ULTRASONIC SURGICAL ASPIRATORValleylab, Inc.K883522AMERIMED ULTRASONIC SURGICAL ASPIRATION KITAmerimed US Corp.K855138BOVIE ULTRASONIC SURGICAL SYSTEMClinical Technology Corp.K853143COOPER LASER SONICS CUSA MODEL 200Cooper Lasersonics, Inc.

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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