Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

INTELECT MODEL 200

K-Number: K813593 · 1982-02-22

ApplicantChattanooga Group, Inc.
Decision Date1982-02-22
Product CodeIMI
Advisory CommitteePM
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 K813593. 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 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 K813593.

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 K813593.

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.

What is the FDA product code for INTELECT MODEL 200?

The FDA product code for INTELECT MODEL 200 is IMI.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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

View all 70 devices →

Related Devices (Code: IMI)

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.

K240788Ultrasound StimulatorJkh Health Co., Ltd.K230472Sonopuls 190Enraf-Nonius, B.V.K222098ManaSport+Manamed, Inc.K210284ManaSportManamed, Inc.K202788Sonomed IV, Sonomed VCarci Industria E Comercio DE Aparelhos Cirurgicos E OrtoK160378BRH-A2 Combined Ultrasound and Electric Field Stimulation (CUSEFS)Brh Medical , Ltd.

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.

↑