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FDA 510(k)

MEDIUM FREQ. ELECTRICAL MUSCLE STIMULA

K-Number: K841598 · 1984-05-10

ApplicantChattanooga Group, Inc.
Decision Date1984-05-10
Product Code
DecisionSubstantially Equivalent

Device Summary

MEDIUM FREQ. ELECTRICAL MUSCLE STIMULA 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 1984-05-10 under 510(k) number K841598. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDIUM FREQ. ELECTRICAL MUSCLE STIMULA?

MEDIUM FREQ. ELECTRICAL MUSCLE STIMULA is a medical device that received FDA 510(k) clearance on 1984-05-10. The listed applicant is Chattanooga Group, Inc.. The 510(k) number is K841598.

When did MEDIUM FREQ. ELECTRICAL MUSCLE STIMULA receive FDA 510(k) clearance?

MEDIUM FREQ. ELECTRICAL MUSCLE STIMULA received FDA 510(k) clearance on 1984-05-10, under 510(k) number K841598.

Who is the listed applicant for MEDIUM FREQ. ELECTRICAL MUSCLE STIMULA?

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

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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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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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