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FDA 510(k)

INTELECT MODEL 120

K-Number: K880235 · 1988-04-08

ApplicantChattanooga Group, Inc.
Decision Date1988-04-08
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

INTELECT MODEL 120 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 1988-04-08 under 510(k) number K880235. 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 MODEL 120?

INTELECT MODEL 120 is a medical device that received FDA 510(k) clearance on 1988-04-08. The listed applicant is Chattanooga Group, Inc.. The 510(k) number is K880235.

When did INTELECT MODEL 120 receive FDA 510(k) clearance?

INTELECT MODEL 120 received FDA 510(k) clearance on 1988-04-08, under 510(k) number K880235.

Who is the listed applicant for INTELECT MODEL 120?

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 120?

The FDA product code for INTELECT MODEL 120 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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