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FDA 510(k)

FORTE, MODEL CPS ULTRASOUND

K-Number: K982829 · 1998-11-06

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

Device Summary

FORTE, MODEL CPS ULTRASOUND 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 K982829. The device is classified under product code IMI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FORTE, MODEL CPS ULTRASOUND?

FORTE, MODEL CPS ULTRASOUND 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 K982829.

When did FORTE, MODEL CPS ULTRASOUND receive FDA 510(k) clearance?

FORTE, MODEL CPS ULTRASOUND received FDA 510(k) clearance on 1998-11-06, under 510(k) number K982829.

Who is the listed applicant for FORTE, MODEL CPS ULTRASOUND?

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, MODEL CPS ULTRASOUND?

The FDA product code for FORTE, MODEL CPS ULTRASOUND is IMI.

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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.

K011243CHATTANOOGA DRY HEAT WHIRLPOOL, MODEL 2000K982317VECTRA COMBOK982321VECTRA STIM MODELS 200 AND 400K982324VECTRA PRO MODELS 2 AND 4K982828FORTE, MODELS CPS 400 STIM, CPS 200 STIMK982830FORTE, MODELS CPS 400 COMBO, CPS 200 COMBO

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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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