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FDA 510(k)

INTELECT MODEL 200

K-Number: K827034 · 1982-02-22

ApplicantChattanooga Group, Inc.
Decision Date1982-02-22
Product Code
DecisionSubstantially Equivalent

Device Summary

INTELECT MODEL 200 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 1982-02-22 under 510(k) number K827034. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTELECT MODEL 200?

INTELECT MODEL 200 is a medical device that received FDA 510(k) clearance on 1982-02-22. The listed applicant is Chattanooga Group, Inc.. The 510(k) number is K827034.

When did INTELECT MODEL 200 receive FDA 510(k) clearance?

INTELECT MODEL 200 received FDA 510(k) clearance on 1982-02-22, under 510(k) number K827034.

Who is the listed applicant for INTELECT MODEL 200?

The FDA 510(k) record lists Chattanooga Group, Inc. as the applicant. This does not by itself establish the device manufacturer.

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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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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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