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FDA 510(k)

HEARING AID (ALL-IN-THE-EAR) MODEL WORD SORTER

K-Number: K874764 · 1987-12-10

ApplicantClear Corp.
Decision Date1987-12-10
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

HEARING AID (ALL-IN-THE-EAR) MODEL WORD SORTER is the device name listed in this FDA 510(k) record. The listed applicant is Clear Corp.. It received FDA 510(k) clearance on 1987-12-10 under 510(k) number K874764. 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 HEARING AID (ALL-IN-THE-EAR) MODEL WORD SORTER?

HEARING AID (ALL-IN-THE-EAR) MODEL WORD SORTER is a medical device that received FDA 510(k) clearance on 1987-12-10. The listed applicant is Clear Corp.. The 510(k) number is K874764.

When did HEARING AID (ALL-IN-THE-EAR) MODEL WORD SORTER receive FDA 510(k) clearance?

HEARING AID (ALL-IN-THE-EAR) MODEL WORD SORTER received FDA 510(k) clearance on 1987-12-10, under 510(k) number K874764.

Who is the listed applicant for HEARING AID (ALL-IN-THE-EAR) MODEL WORD SORTER?

The FDA 510(k) record lists Clear Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEARING AID (ALL-IN-THE-EAR) MODEL WORD SORTER?

The FDA product code for HEARING AID (ALL-IN-THE-EAR) MODEL WORD SORTER is ESD.

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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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