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FDA 510(k)

VECTORSURGE 5 MODEL 470

K-Number: K030648 · 2003-03-28

ApplicantMetron Medical Australia, Pty, Ltd.
Decision Date2003-03-28
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

VECTORSURGE 5 MODEL 470 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 2003-03-28 under 510(k) number K030648. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VECTORSURGE 5 MODEL 470?

VECTORSURGE 5 MODEL 470 is a medical device that received FDA 510(k) clearance on 2003-03-28. The listed applicant is Metron Medical Australia, Pty, Ltd.. The 510(k) number is K030648.

When did VECTORSURGE 5 MODEL 470 receive FDA 510(k) clearance?

VECTORSURGE 5 MODEL 470 received FDA 510(k) clearance on 2003-03-28, under 510(k) number K030648.

Who is the listed applicant for VECTORSURGE 5 MODEL 470?

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 VECTORSURGE 5 MODEL 470?

The FDA product code for VECTORSURGE 5 MODEL 470 is IPF.

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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-270K030878ACCOUSONIC, MODEL AS-270K030410ACCOUSONIC PLUS, MODEL AP-170

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Related Devices (Code: IPF)

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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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