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FDA 510(k)

MULTI-STIM, MODEL MS-100

K-Number: K001897 · 2001-06-12

ApplicantMetron Medical Australia, Pty, Ltd.
Decision Date2001-06-12
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MULTI-STIM, MODEL MS-100 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 2001-06-12 under 510(k) number K001897. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTI-STIM, MODEL MS-100?

MULTI-STIM, MODEL MS-100 is a medical device that received FDA 510(k) clearance on 2001-06-12. The listed applicant is Metron Medical Australia, Pty, Ltd.. The 510(k) number is K001897.

When did MULTI-STIM, MODEL MS-100 receive FDA 510(k) clearance?

MULTI-STIM, MODEL MS-100 received FDA 510(k) clearance on 2001-06-12, under 510(k) number K001897.

Who is the listed applicant for MULTI-STIM, MODEL MS-100?

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 MULTI-STIM, MODEL MS-100?

The FDA product code for MULTI-STIM, MODEL MS-100 is GZJ.

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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.

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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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