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FDA 510(k)

INTELECT 750 MP

K-Number: K902875 · 1990-09-27

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

Device Summary

INTELECT 750 MP 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 K902875. 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 750 MP?

INTELECT 750 MP 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 K902875.

When did INTELECT 750 MP receive FDA 510(k) clearance?

INTELECT 750 MP received FDA 510(k) clearance on 1990-09-27, under 510(k) number K902875.

Who is the listed applicant for INTELECT 750 MP?

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 750 MP?

The FDA product code for INTELECT 750 MP is IMG.

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Other records listing Chattanooga Group, Inc. as applicant

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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.

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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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