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FDA 510(k)

ELECTRO-GONIOMETER

K-Number: K812908 · 1981-11-24

ApplicantChattanooga Group, Inc.
Decision Date1981-11-24
Product CodeKQX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ELECTRO-GONIOMETER 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 1981-11-24 under 510(k) number K812908. The device is classified under product code KQX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRO-GONIOMETER?

ELECTRO-GONIOMETER is a medical device that received FDA 510(k) clearance on 1981-11-24. The listed applicant is Chattanooga Group, Inc.. The 510(k) number is K812908.

When did ELECTRO-GONIOMETER receive FDA 510(k) clearance?

ELECTRO-GONIOMETER received FDA 510(k) clearance on 1981-11-24, under 510(k) number K812908.

Who is the listed applicant for ELECTRO-GONIOMETER?

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 ELECTRO-GONIOMETER?

The FDA product code for ELECTRO-GONIOMETER is KQX.

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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: KQX)

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.

K011827ORTELIUS 800Orthoscan , Ltd.K971079INTERLOGICS W-TRACKER AND WRIST WORKS SOFTWAREInterlogics, Inc.K9623773D-SPINESkill Technologies, Inc.K961212SPINAL TOUCHFasstechK954647INCLINOMETERJ-Tech, Inc.K943929DATAGLOVE AND MOVEMENT ANALYSIS SYSTEM (MAS)Greenleaf Medical Systems, Inc.

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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