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FDA 510(k)

FACEPLATE ITE HEARING AID MODEL TCA

K-Number: K910900 · 1991-05-30

ApplicantTelex Communications, Inc.
Decision Date1991-05-30
Product CodeLRB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

FACEPLATE ITE HEARING AID MODEL TCA is the device name listed in this FDA 510(k) record. The listed applicant is Telex Communications, Inc.. It received FDA 510(k) clearance on 1991-05-30 under 510(k) number K910900. The device is classified under product code LRB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FACEPLATE ITE HEARING AID MODEL TCA?

FACEPLATE ITE HEARING AID MODEL TCA is a medical device that received FDA 510(k) clearance on 1991-05-30. The listed applicant is Telex Communications, Inc.. The 510(k) number is K910900.

When did FACEPLATE ITE HEARING AID MODEL TCA receive FDA 510(k) clearance?

FACEPLATE ITE HEARING AID MODEL TCA received FDA 510(k) clearance on 1991-05-30, under 510(k) number K910900.

Who is the listed applicant for FACEPLATE ITE HEARING AID MODEL TCA?

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

What is the FDA product code for FACEPLATE ITE HEARING AID MODEL TCA?

The FDA product code for FACEPLATE ITE HEARING AID MODEL TCA is LRB.

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Other records listing Telex Communications, 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.

K984243TELEX TINNITUS-COMPANIONK982683TELEX SELECT 1-40 WITH ADAPTIVE COMPRESSIONK964639TELEX IN-THE-EAR CUSTOM HEARING AID WITH THRESHOLD COMPRESSION-IIK963915TELEX IN-THE-EAR CUSTOM HEARING AID WITH THRESHOLD COMPRESSIONK961143TELEX SELECT 2-40 WITH ADAPTIVE COMPRESSION S2-40K954579TELEX 349 MULTI CROS W/ADAPIVE COMPRESSION

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Related Devices (Code: LRB)

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.

K974219FACEPLATE ASSEMBLYFinetone Hearing InstrumentsK961593INTRASTAR PRE-WIRED FACEPLATE FOR IN-THE-EAR HEARING AIDSSegi Hearing Aid Co.K942722MODULE PROGRAMElectone, Inc.K942236AUDINA PREWIRES (FACEPLATE HEARING AID SERIES)Audina Hearing InstrumentK935048ARTISAN PROGRAMMER & HEARING AIDTelex Communications, Inc.K933046SILVER L MODULE, ITEElectone, Inc.

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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