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FDA 510(k)

INTELECT IFC2

K-Number: K924666 · 1993-03-05

ApplicantChattanooga Group, Inc.
Decision Date1993-03-05
Product CodeLIH
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

INTELECT IFC2 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 1993-03-05 under 510(k) number K924666. The device is classified under product code LIH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTELECT IFC2?

INTELECT IFC2 is a medical device that received FDA 510(k) clearance on 1993-03-05. The listed applicant is Chattanooga Group, Inc.. The 510(k) number is K924666.

When did INTELECT IFC2 receive FDA 510(k) clearance?

INTELECT IFC2 received FDA 510(k) clearance on 1993-03-05, under 510(k) number K924666.

Who is the listed applicant for INTELECT IFC2?

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 IFC2?

The FDA product code for INTELECT IFC2 is LIH.

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Other records listing Chattanooga Group, Inc. as applicant

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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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