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FDA 510(k)

STARKEY TRILOGY PROGRAM HEAR AID CC/CE MODELS

K-Number: K911579 · 1991-05-07

ApplicantStarkey Laboratories, Inc.
Decision Date1991-05-07
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

STARKEY TRILOGY PROGRAM HEAR AID CC/CE MODELS is the device name listed in this FDA 510(k) record. The listed applicant is Starkey Laboratories, Inc.. It received FDA 510(k) clearance on 1991-05-07 under 510(k) number K911579. The device is classified under product code ESD. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STARKEY TRILOGY PROGRAM HEAR AID CC/CE MODELS?

STARKEY TRILOGY PROGRAM HEAR AID CC/CE MODELS is a medical device that received FDA 510(k) clearance on 1991-05-07. The listed applicant is Starkey Laboratories, Inc.. The 510(k) number is K911579.

When did STARKEY TRILOGY PROGRAM HEAR AID CC/CE MODELS receive FDA 510(k) clearance?

STARKEY TRILOGY PROGRAM HEAR AID CC/CE MODELS received FDA 510(k) clearance on 1991-05-07, under 510(k) number K911579.

Who is the listed applicant for STARKEY TRILOGY PROGRAM HEAR AID CC/CE MODELS?

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

What is the FDA product code for STARKEY TRILOGY PROGRAM HEAR AID CC/CE MODELS?

The FDA product code for STARKEY TRILOGY PROGRAM HEAR AID CC/CE MODELS is ESD.

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Other records listing Starkey Laboratories, 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.

K201370Multiflex Tinnitus TechnologyK030180CRESCENT TINNITUS RETAINING SOUND GENERATORK970952PRECISE IMPRESSION KITK964245PRECISE, TYNMPANETTE, AND XACTO IMPRESSION KITSK964340PORTAREM-3000, PFS-6000K964216STARKEY TM-3, TM-5 HIGH FREQUENCY TINNITUS MASKER

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Related Devices (Code: ESD)

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.

K232999Lyric4 Hearing AidSonova AGK130790LYRIC2Phonak, LLCK081136LYRIC HEARING AIDInsound Medical, Inc.K021867INSOUND XT SERIES HEARING AIDInsound Medical, Inc.K003558TCI COMBI (TINNITUS CONTROL INSTRUMENT COMBINATION)Siemens Hearing Instruments, Inc.K984518SONIC INNOVATIONS COMPLETELY-IN-THE-CANAL DSP HEARING AID WITH SOFT SHELLSonic Innovations, 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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