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FDA 510(k)

MED-EX

K-Number: K812899 · 1981-11-06

ApplicantChattanooga Group, Inc.
Decision Date1981-11-06
Product CodeLBB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MED-EX 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 1981-11-06 under 510(k) number K812899. The device is classified under product code LBB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MED-EX?

MED-EX is a medical device that received FDA 510(k) clearance on 1981-11-06. The listed applicant is Chattanooga Group, Inc.. The 510(k) number is K812899.

When did MED-EX receive FDA 510(k) clearance?

MED-EX received FDA 510(k) clearance on 1981-11-06, under 510(k) number K812899.

Who is the listed applicant for MED-EX?

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 MED-EX?

The FDA product code for MED-EX is LBB.

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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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