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FDA 510(k)

SONIC MODEL SO-300

K-Number: K010102 · 2001-02-09

Decision Date2001-02-09
Product CodeIMI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SONIC MODEL SO-300 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 2001-02-09 under 510(k) number K010102. The device is classified under product code IMI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SONIC MODEL SO-300?

SONIC MODEL SO-300 is a medical device that received FDA 510(k) clearance on 2001-02-09. The listed applicant is Metron Medical Australia, Pty, Ltd.. The 510(k) number is K010102.

When did SONIC MODEL SO-300 receive FDA 510(k) clearance?

SONIC MODEL SO-300 received FDA 510(k) clearance on 2001-02-09, under 510(k) number K010102.

Who is the listed applicant for SONIC MODEL SO-300?

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 SONIC MODEL SO-300?

The FDA product code for SONIC MODEL SO-300 is IMI.

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 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.

View all 17 devices →

Related Devices (Code: IMI)

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

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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