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FDA 510(k)

INTELECT 600MP

K-Number: K920260 · 1992-10-13

ApplicantChattanooga Group, Inc.
Decision Date1992-10-13
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

INTELECT 600MP 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 1992-10-13 under 510(k) number K920260. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTELECT 600MP?

INTELECT 600MP is a medical device that received FDA 510(k) clearance on 1992-10-13. The listed applicant is Chattanooga Group, Inc.. The 510(k) number is K920260.

When did INTELECT 600MP receive FDA 510(k) clearance?

INTELECT 600MP received FDA 510(k) clearance on 1992-10-13, under 510(k) number K920260.

Who is the listed applicant for INTELECT 600MP?

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 600MP?

The FDA product code for INTELECT 600MP is GZJ.

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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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