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FDA 510(k)

VECTORSONIC, MODEL VU-200

K-Number: K020119 · 2002-07-22

ApplicantMetron Medical Australia, Pty, Ltd.
Decision Date2002-07-22
Product CodeIMG
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

VECTORSONIC, MODEL VU-200 is the device name listed in this FDA 510(k) record. The listed applicant is Metron Medical Australia, Pty, Ltd.. It received FDA 510(k) clearance on 2002-07-22 under 510(k) number K020119. The device is classified under product code IMG. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VECTORSONIC, MODEL VU-200?

VECTORSONIC, MODEL VU-200 is a medical device that received FDA 510(k) clearance on 2002-07-22. The listed applicant is Metron Medical Australia, Pty, Ltd.. The 510(k) number is K020119.

When did VECTORSONIC, MODEL VU-200 receive FDA 510(k) clearance?

VECTORSONIC, MODEL VU-200 received FDA 510(k) clearance on 2002-07-22, under 510(k) number K020119.

Who is the listed applicant for VECTORSONIC, MODEL VU-200?

The FDA 510(k) record lists Metron Medical Australia, Pty, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VECTORSONIC, MODEL VU-200?

The FDA product code for VECTORSONIC, MODEL VU-200 is IMG.

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Other records listing Metron Medical Australia, Pty, Ltd. 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.

K132137MULTISTIMK124010ACCUSONIC ADVANTAGEK120171ACCUSONIC ADVANTAGEK030880VECTORSONIC, MODEL VU-270K030648VECTORSURGE 5 MODEL 470K030878ACCOUSONIC, MODEL AS-270

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Related Devices (Code: IMG)

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.

K244041Ultrasound Therapy Workstation (XMS-UET2)Xemis Medical Technology (Shenzhen) Co., Ltd.K153559OmniVersa Multi-Modality Therapy System and Omnistim FX2 Professional Therapy SystemAccelerated Care Plus (Acp)K120217SONICSTIMU COMBO THERAPEUTIC DEVICEShenzhen Dongdixin Technology Co., Ltd.K121059SOLEOLINE, SOLEO STIM, SOLEO SONO, SOLEO SONOSTIMZimmer Medizinsystems GmbHK102524FUTURADr. Oliver Wenker, M.D., M.B.A.K111482SONICATOR PLUS 920Mettler Electronics Corp.

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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