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FDA 510(k)

KC/EMG DIAGNOSTIC ELECTROMYOGRAPH

K-Number: K864630 · 1986-12-29

ApplicantChattanooga Group, Inc.
Decision Date1986-12-29
Product CodeIKN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

KC/EMG DIAGNOSTIC ELECTROMYOGRAPH 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 1986-12-29 under 510(k) number K864630. The device is classified under product code IKN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KC/EMG DIAGNOSTIC ELECTROMYOGRAPH?

KC/EMG DIAGNOSTIC ELECTROMYOGRAPH is a medical device that received FDA 510(k) clearance on 1986-12-29. The listed applicant is Chattanooga Group, Inc.. The 510(k) number is K864630.

When did KC/EMG DIAGNOSTIC ELECTROMYOGRAPH receive FDA 510(k) clearance?

KC/EMG DIAGNOSTIC ELECTROMYOGRAPH received FDA 510(k) clearance on 1986-12-29, under 510(k) number K864630.

Who is the listed applicant for KC/EMG DIAGNOSTIC ELECTROMYOGRAPH?

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 KC/EMG DIAGNOSTIC ELECTROMYOGRAPH?

The FDA product code for KC/EMG DIAGNOSTIC ELECTROMYOGRAPH is IKN.

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Other records listing Chattanooga Group, Inc. as applicant

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Related Devices (Code: IKN)

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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