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FDA 510(k)

TTCGHI-T AND TTCTN3-T-T

K-Number: K982451 · 1999-05-07

ApplicantTinnitus Treatment Centers, Inc.
Decision Date1999-05-07
Product CodeKLW
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

TTCGHI-T AND TTCTN3-T-T is the device name listed in this FDA 510(k) record. The listed applicant is Tinnitus Treatment Centers, Inc.. It received FDA 510(k) clearance on 1999-05-07 under 510(k) number K982451. The device is classified under product code KLW. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TTCGHI-T AND TTCTN3-T-T?

TTCGHI-T AND TTCTN3-T-T is a medical device that received FDA 510(k) clearance on 1999-05-07. The listed applicant is Tinnitus Treatment Centers, Inc.. The 510(k) number is K982451.

When did TTCGHI-T AND TTCTN3-T-T receive FDA 510(k) clearance?

TTCGHI-T AND TTCTN3-T-T received FDA 510(k) clearance on 1999-05-07, under 510(k) number K982451.

Who is the listed applicant for TTCGHI-T AND TTCTN3-T-T?

The FDA 510(k) record lists Tinnitus Treatment Centers, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TTCGHI-T AND TTCTN3-T-T?

The FDA product code for TTCGHI-T AND TTCTN3-T-T is KLW.

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.

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Other records listing Tinnitus Treatment Centers, 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.

K982432PILLOW MASKER, C2007M, C2008M,CE2000, WONDER EAR, MINI WONDER EAR, PT-2SM, PT-3SM, PT-3LFM, PT-3HFM, PT3CM, PT5-SM, PT5-

Related Devices (Code: KLW)

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.

K260413Levo Gen 2 Tinnitus Therapy SystemLevo Medical CorporationK260614Tinnitus TherapySivantos GmbHK233435Peace N Quiet (0.7.0)Pnq HealthK223694Tinearity G1 (6103); Tinearity G1 Adapters x3 (6042)Duearity ABK221168Tinnitogram Signal GeneratorGoldenear Company, Inc.K221125SilentCloudAureliym GmbH

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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