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FDA 510(k)

MOBILIZATIOIN TABLE

K-Number: K841594 · 1984-05-09

ApplicantChattanooga Group, Inc.
Decision Date1984-05-09
Product CodeINQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MOBILIZATIOIN TABLE 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 1984-05-09 under 510(k) number K841594. The device is classified under product code INQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOBILIZATIOIN TABLE?

MOBILIZATIOIN TABLE is a medical device that received FDA 510(k) clearance on 1984-05-09. The listed applicant is Chattanooga Group, Inc.. The 510(k) number is K841594.

When did MOBILIZATIOIN TABLE receive FDA 510(k) clearance?

MOBILIZATIOIN TABLE received FDA 510(k) clearance on 1984-05-09, under 510(k) number K841594.

Who is the listed applicant for MOBILIZATIOIN TABLE?

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 MOBILIZATIOIN TABLE?

The FDA product code for MOBILIZATIOIN TABLE is INQ.

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Related Devices (Code: INQ)

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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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