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FDA 510(k)

THE SOUNDVASER DISSECTION SYSTEM

K-Number: K993868 · 1999-12-21

Decision Date1999-12-21
Product CodeLFL
DecisionSubstantially Equivalent

Device Summary

THE SOUNDVASER DISSECTION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Sound Surgical Technologies, LLC. It received FDA 510(k) clearance on 1999-12-21 under 510(k) number K993868. The device is classified under product code LFL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE SOUNDVASER DISSECTION SYSTEM?

THE SOUNDVASER DISSECTION SYSTEM is a medical device that received FDA 510(k) clearance on 1999-12-21. The listed applicant is Sound Surgical Technologies, LLC. The 510(k) number is K993868.

When did THE SOUNDVASER DISSECTION SYSTEM receive FDA 510(k) clearance?

THE SOUNDVASER DISSECTION SYSTEM received FDA 510(k) clearance on 1999-12-21, under 510(k) number K993868.

Who is the listed applicant for THE SOUNDVASER DISSECTION SYSTEM?

The FDA 510(k) record lists Sound Surgical Technologies, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE SOUNDVASER DISSECTION SYSTEM?

The FDA product code for THE SOUNDVASER DISSECTION SYSTEM is LFL.

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 Sound Surgical Technologies, LLC 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.

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.

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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