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FDA 510(k)

CUSA SYSTEM 200H ULTRASONIC SURGICAL ASPIRATOR

K-Number: K884413 · 1988-12-02

Decision Date1988-12-02
Product CodeLBK
DecisionSubstantially Equivalent

Device Summary

CUSA SYSTEM 200H ULTRASONIC SURGICAL 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 1988-12-02 under 510(k) number K884413. The device is classified under product code LBK. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CUSA SYSTEM 200H ULTRASONIC SURGICAL ASPIRATOR?

CUSA SYSTEM 200H ULTRASONIC SURGICAL ASPIRATOR 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 K884413.

When did CUSA SYSTEM 200H ULTRASONIC SURGICAL ASPIRATOR receive FDA 510(k) clearance?

CUSA SYSTEM 200H ULTRASONIC SURGICAL ASPIRATOR received FDA 510(k) clearance on 1988-12-02, under 510(k) number K884413.

Who is the listed applicant for CUSA SYSTEM 200H ULTRASONIC SURGICAL 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 SYSTEM 200H ULTRASONIC SURGICAL ASPIRATOR?

The FDA product code for CUSA SYSTEM 200H ULTRASONIC SURGICAL ASPIRATOR is LBK.

Related Clinical Trials

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.

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.

View all 94 devices →

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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