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FDA 510(k)

FORTE ES

K-Number: K940759 · 1995-03-16

ApplicantChattanooga Group, Inc.
Decision Date1995-03-16
Product CodeGZI
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

FORTE ES 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 1995-03-16 under 510(k) number K940759. The device is classified under product code GZI. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FORTE ES?

FORTE ES is a medical device that received FDA 510(k) clearance on 1995-03-16. The listed applicant is Chattanooga Group, Inc.. The 510(k) number is K940759.

When did FORTE ES receive FDA 510(k) clearance?

FORTE ES received FDA 510(k) clearance on 1995-03-16, under 510(k) number K940759.

Who is the listed applicant for FORTE ES?

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 ES?

The FDA product code for FORTE ES is GZI.

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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 STIMK982829FORTE, MODEL CPS ULTRASOUND

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Related Devices (Code: GZI)

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

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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