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FDA 510(k)

EMG RETRAINER

K-Number: K972487 · 1997-09-26

ApplicantChattanooga Group, Inc.
Decision Date1997-09-26
Product CodeHCC
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

EMG RETRAINER is the device name listed in this FDA 510(k) record. The listed applicant is Chattanooga Group, Inc.. It received FDA 510(k) clearance on 1997-09-26 under 510(k) number K972487. 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 RETRAINER?

EMG RETRAINER is a medical device that received FDA 510(k) clearance on 1997-09-26. The listed applicant is Chattanooga Group, Inc.. The 510(k) number is K972487.

When did EMG RETRAINER receive FDA 510(k) clearance?

EMG RETRAINER received FDA 510(k) clearance on 1997-09-26, under 510(k) number K972487.

Who is the listed applicant for EMG RETRAINER?

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

What is the FDA product code for EMG RETRAINER?

The FDA product code for EMG RETRAINER is HCC.

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Other records listing Chattanooga Group, Inc. 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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Related Devices (Code: HCC)

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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