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FDA 510(k)

EMG BIOFEEDBACK DEVICE

K-Number: K823511 · 1983-03-31

ApplicantNemectron Medical, Inc.
Decision Date1983-03-31
Product CodeHCC
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

EMG BIOFEEDBACK DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Nemectron Medical, Inc.. It received FDA 510(k) clearance on 1983-03-31 under 510(k) number K823511. The device is classified under product code HCC. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EMG BIOFEEDBACK DEVICE?

EMG BIOFEEDBACK DEVICE is a medical device that received FDA 510(k) clearance on 1983-03-31. The listed applicant is Nemectron Medical, Inc.. The 510(k) number is K823511.

When did EMG BIOFEEDBACK DEVICE receive FDA 510(k) clearance?

EMG BIOFEEDBACK DEVICE received FDA 510(k) clearance on 1983-03-31, under 510(k) number K823511.

Who is the listed applicant for EMG BIOFEEDBACK DEVICE?

The FDA 510(k) record lists Nemectron Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EMG BIOFEEDBACK DEVICE?

The FDA product code for EMG BIOFEEDBACK DEVICE is HCC.

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Other records listing Nemectron Medical, Inc. as applicant

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Related Devices (Code: HCC)

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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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