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FDA 510(k)

BALANCE SYSTEM

K-Number: K884926 · 1989-02-27

Decision Date1989-02-27
Product CodeLXV
DecisionSubstantially Equivalent

Device Summary

BALANCE SYSTEM 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 1989-02-27 under 510(k) number K884926. The device is classified under product code LXV. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BALANCE SYSTEM?

BALANCE SYSTEM is a medical device that received FDA 510(k) clearance on 1989-02-27. The listed applicant is Chattanooga Group, Inc.. The 510(k) number is K884926.

When did BALANCE SYSTEM receive FDA 510(k) clearance?

BALANCE SYSTEM received FDA 510(k) clearance on 1989-02-27, under 510(k) number K884926.

Who is the listed applicant for BALANCE SYSTEM?

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 BALANCE SYSTEM?

The FDA product code for BALANCE SYSTEM is LXV.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Chattanooga Group, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: LXV)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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