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FDA 510(k)

ALLIGER ULTRASONIC SURGICAL SYSTEM

K-Number: K933559 · 1993-10-15

Decision Date1993-10-15
Product CodeLFL
DecisionSubstantially Equivalent

Device Summary

ALLIGER ULTRASONIC SURGICAL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medsonic, Inc.. It received FDA 510(k) clearance on 1993-10-15 under 510(k) number K933559. The device is classified under product code LFL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALLIGER ULTRASONIC SURGICAL SYSTEM?

ALLIGER ULTRASONIC SURGICAL SYSTEM is a medical device that received FDA 510(k) clearance on 1993-10-15. The listed applicant is Medsonic, Inc.. The 510(k) number is K933559.

When did ALLIGER ULTRASONIC SURGICAL SYSTEM receive FDA 510(k) clearance?

ALLIGER ULTRASONIC SURGICAL SYSTEM received FDA 510(k) clearance on 1993-10-15, under 510(k) number K933559.

Who is the listed applicant for ALLIGER ULTRASONIC SURGICAL SYSTEM?

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

What is the FDA product code for ALLIGER ULTRASONIC SURGICAL SYSTEM?

The FDA product code for ALLIGER ULTRASONIC SURGICAL 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.

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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