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FDA 510(k)

INTELECT 170

K-Number: K902860 · 1990-09-27

ApplicantChattanooga Group, Inc.
Decision Date1990-09-27
Product CodeIMG
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

INTELECT 170 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 1990-09-27 under 510(k) number K902860. The device is classified under product code IMG. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTELECT 170?

INTELECT 170 is a medical device that received FDA 510(k) clearance on 1990-09-27. The listed applicant is Chattanooga Group, Inc.. The 510(k) number is K902860.

When did INTELECT 170 receive FDA 510(k) clearance?

INTELECT 170 received FDA 510(k) clearance on 1990-09-27, under 510(k) number K902860.

Who is the listed applicant for INTELECT 170?

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 170?

The FDA product code for INTELECT 170 is IMG.

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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.

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Related Devices (Code: IMG)

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.

K244041Ultrasound Therapy Workstation (XMS-UET2)Xemis Medical Technology (Shenzhen) Co., Ltd.K153559OmniVersa Multi-Modality Therapy System and Omnistim FX2 Professional Therapy SystemAccelerated Care Plus (Acp)K120217SONICSTIMU COMBO THERAPEUTIC DEVICEShenzhen Dongdixin Technology Co., Ltd.K121059SOLEOLINE, SOLEO STIM, SOLEO SONO, SOLEO SONOSTIMZimmer Medizinsystems GmbHK102524FUTURADr. Oliver Wenker, M.D., M.B.A.K111482SONICATOR PLUS 920Mettler Electronics 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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