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FDA 510(k)

ELECTRO-GONIOMETER DIAGNOSTIC DEVICE

K-Number: K901290 · 1990-10-01

ApplicantChattanooga Group, Inc.
Decision Date1990-10-01
Product CodeLBB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ELECTRO-GONIOMETER DIAGNOSTIC DEVICE 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 1990-10-01 under 510(k) number K901290. The device is classified under product code LBB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECTRO-GONIOMETER DIAGNOSTIC DEVICE?

ELECTRO-GONIOMETER DIAGNOSTIC DEVICE is a medical device that received FDA 510(k) clearance on 1990-10-01. The listed applicant is Chattanooga Group, Inc.. The 510(k) number is K901290.

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

ELECTRO-GONIOMETER DIAGNOSTIC DEVICE received FDA 510(k) clearance on 1990-10-01, under 510(k) number K901290.

Who is the listed applicant for ELECTRO-GONIOMETER DIAGNOSTIC DEVICE?

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 DIAGNOSTIC DEVICE?

The FDA product code for ELECTRO-GONIOMETER DIAGNOSTIC DEVICE is LBB.

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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 4K982830FORTE, MODELS CPS 400 COMBO, CPS 200 COMBOK982828FORTE, MODELS CPS 400 STIM, CPS 200 STIM

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Related Devices (Code: LBB)

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.

K162412Hoggan Scientific® microFET2™Hoggan Scientific, LLCK073154FACTS HAND AND PINCH GRIP COMBOGlobal Services Group, LLCK052309DIGITAL HAND DYNAMOMETER, MODEL SH5003; DIGITAL PINCH GAUGE, MODEL SH5006Saehan Corp.K042889DYNAMOMETER - MODEL FCE AND MODEL MSCAmetekK012492KADANCE 2000Kada Research, Inc.K981730DIGIT-GRIP WITH LCD, MODEL NUMBER DGR 002Nk Biotechnical Corp.

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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