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FDA 510(k)

EMG REPORT GENERATOR

K-Number: K844681 · 1985-02-26

ApplicantMicrosystem Controls
Decision Date1985-02-26
Product CodeJXE
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

EMG REPORT GENERATOR is the device name listed in this FDA 510(k) record. The listed applicant is Microsystem Controls. It received FDA 510(k) clearance on 1985-02-26 under 510(k) number K844681. The device is classified under product code JXE. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EMG REPORT GENERATOR?

EMG REPORT GENERATOR is a medical device that received FDA 510(k) clearance on 1985-02-26. The listed applicant is Microsystem Controls. The 510(k) number is K844681.

When did EMG REPORT GENERATOR receive FDA 510(k) clearance?

EMG REPORT GENERATOR received FDA 510(k) clearance on 1985-02-26, under 510(k) number K844681.

Who is the listed applicant for EMG REPORT GENERATOR?

The FDA 510(k) record lists Microsystem Controls as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EMG REPORT GENERATOR?

The FDA product code for EMG REPORT GENERATOR is JXE.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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