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FDA 510(k)

INTELECT 775

K-Number: K872655 · 1987-11-03

ApplicantChattanooga Group, Inc.
Decision Date1987-11-03
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

INTELECT 775 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 1987-11-03 under 510(k) number K872655. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTELECT 775?

INTELECT 775 is a medical device that received FDA 510(k) clearance on 1987-11-03. The listed applicant is Chattanooga Group, Inc.. The 510(k) number is K872655.

When did INTELECT 775 receive FDA 510(k) clearance?

INTELECT 775 received FDA 510(k) clearance on 1987-11-03, under 510(k) number K872655.

Who is the listed applicant for INTELECT 775?

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 775?

The FDA product code for INTELECT 775 is IPF.

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Other records listing Chattanooga Group, Inc. as applicant

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Related Devices (Code: IPF)

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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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