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FDA 510(k)

HIGH VOLTAGE GALVANIC STIMULATOR 550

K-Number: K813456 · 1982-01-29

ApplicantChattanooga Group, Inc.
Decision Date1982-01-29
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HIGH VOLTAGE GALVANIC STIMULATOR 550 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 1982-01-29 under 510(k) number K813456. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HIGH VOLTAGE GALVANIC STIMULATOR 550?

HIGH VOLTAGE GALVANIC STIMULATOR 550 is a medical device that received FDA 510(k) clearance on 1982-01-29. The listed applicant is Chattanooga Group, Inc.. The 510(k) number is K813456.

When did HIGH VOLTAGE GALVANIC STIMULATOR 550 receive FDA 510(k) clearance?

HIGH VOLTAGE GALVANIC STIMULATOR 550 received FDA 510(k) clearance on 1982-01-29, under 510(k) number K813456.

Who is the listed applicant for HIGH VOLTAGE GALVANIC STIMULATOR 550?

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 HIGH VOLTAGE GALVANIC STIMULATOR 550?

The FDA product code for HIGH VOLTAGE GALVANIC STIMULATOR 550 is IPF.

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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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