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FDA 510(k)

FORTE, MODELS CPS 400 STIM, CPS 200 STIM

K-Number: K982828 · 1998-11-06

ApplicantChattanooga Group, Inc.
Decision Date1998-11-06
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FORTE, MODELS CPS 400 STIM, CPS 200 STIM 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 1998-11-06 under 510(k) number K982828. 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 FORTE, MODELS CPS 400 STIM, CPS 200 STIM?

FORTE, MODELS CPS 400 STIM, CPS 200 STIM is a medical device that received FDA 510(k) clearance on 1998-11-06. The listed applicant is Chattanooga Group, Inc.. The 510(k) number is K982828.

When did FORTE, MODELS CPS 400 STIM, CPS 200 STIM receive FDA 510(k) clearance?

FORTE, MODELS CPS 400 STIM, CPS 200 STIM received FDA 510(k) clearance on 1998-11-06, under 510(k) number K982828.

Who is the listed applicant for FORTE, MODELS CPS 400 STIM, CPS 200 STIM?

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 FORTE, MODELS CPS 400 STIM, CPS 200 STIM?

The FDA product code for FORTE, MODELS CPS 400 STIM, CPS 200 STIM is IPF.

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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: 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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