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FDA 510(k)

MEDIUM FREQU. ELEC. MUSCLE STIMULATOR

K-Number: K850698 · 1985-05-17

ApplicantChattanooga Group, Inc.
Decision Date1985-05-17
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MEDIUM FREQU. ELEC. MUSCLE STIMULATOR 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 1985-05-17 under 510(k) number K850698. 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 MEDIUM FREQU. ELEC. MUSCLE STIMULATOR?

MEDIUM FREQU. ELEC. MUSCLE STIMULATOR is a medical device that received FDA 510(k) clearance on 1985-05-17. The listed applicant is Chattanooga Group, Inc.. The 510(k) number is K850698.

When did MEDIUM FREQU. ELEC. MUSCLE STIMULATOR receive FDA 510(k) clearance?

MEDIUM FREQU. ELEC. MUSCLE STIMULATOR received FDA 510(k) clearance on 1985-05-17, under 510(k) number K850698.

Who is the listed applicant for MEDIUM FREQU. ELEC. MUSCLE STIMULATOR?

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 MEDIUM FREQU. ELEC. MUSCLE STIMULATOR?

The FDA product code for MEDIUM FREQU. ELEC. MUSCLE STIMULATOR is IPF.

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Related Devices (Code: 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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