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FDA 510(k)

SEARS MODEL LM9091 IN-THE-EAR HEARING INSTRUMENT

K-Number: K901388 · 1990-04-16

ApplicantMiracle-Ear, Inc.
Decision Date1990-04-16
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

SEARS MODEL LM9091 IN-THE-EAR HEARING INSTRUMENT is the device name listed in this FDA 510(k) record. The listed applicant is Miracle-Ear, Inc.. It received FDA 510(k) clearance on 1990-04-16 under 510(k) number K901388. 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 SEARS MODEL LM9091 IN-THE-EAR HEARING INSTRUMENT?

SEARS MODEL LM9091 IN-THE-EAR HEARING INSTRUMENT is a medical device that received FDA 510(k) clearance on 1990-04-16. The listed applicant is Miracle-Ear, Inc.. The 510(k) number is K901388.

When did SEARS MODEL LM9091 IN-THE-EAR HEARING INSTRUMENT receive FDA 510(k) clearance?

SEARS MODEL LM9091 IN-THE-EAR HEARING INSTRUMENT received FDA 510(k) clearance on 1990-04-16, under 510(k) number K901388.

Who is the listed applicant for SEARS MODEL LM9091 IN-THE-EAR HEARING INSTRUMENT?

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

What is the FDA product code for SEARS MODEL LM9091 IN-THE-EAR HEARING INSTRUMENT?

The FDA product code for SEARS MODEL LM9091 IN-THE-EAR HEARING INSTRUMENT is ESD.

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Other records listing Miracle-Ear, 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.

K972344MIRACLE-EAR DIGITAL BTEK972345DAHLBERG/MIRACLE-EARK972346MIRACLE-EAR ITE DIGITALK970262MULTI-CHANNEL COMPRESSION BTE (SD)K964419MIRACLE - EAR (ITE/ITC/CIC)K965049DAHLBERG (A-554)

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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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