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FDA 510(k)

HIGH SPEED EMG MODULE

K-Number: K031930 · 2004-03-03

ApplicantMedical Measurement Systems B.V.
Decision Date2004-03-03
Product CodeGWF
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

HIGH SPEED EMG MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Medical Measurement Systems B.V.. It received FDA 510(k) clearance on 2004-03-03 under 510(k) number K031930. The device is classified under product code GWF. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HIGH SPEED EMG MODULE?

HIGH SPEED EMG MODULE is a medical device that received FDA 510(k) clearance on 2004-03-03. The listed applicant is Medical Measurement Systems B.V.. The 510(k) number is K031930.

When did HIGH SPEED EMG MODULE receive FDA 510(k) clearance?

HIGH SPEED EMG MODULE received FDA 510(k) clearance on 2004-03-03, under 510(k) number K031930.

Who is the listed applicant for HIGH SPEED EMG MODULE?

The FDA 510(k) record lists Medical Measurement Systems B.V. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HIGH SPEED EMG MODULE?

The FDA product code for HIGH SPEED EMG MODULE is GWF.

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Other records listing Medical Measurement Systems B.V. 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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