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FDA 510(k)

POST-AURICULAR HEARING AID MODEL PE 805 SCD2

K-Number: K872474 · 1987-07-28

ApplicantPhonic Ear, Inc.
Decision Date1987-07-28
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

POST-AURICULAR HEARING AID MODEL PE 805 SCD2 is the device name listed in this FDA 510(k) record. The listed applicant is Phonic Ear, Inc.. It received FDA 510(k) clearance on 1987-07-28 under 510(k) number K872474. 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 POST-AURICULAR HEARING AID MODEL PE 805 SCD2?

POST-AURICULAR HEARING AID MODEL PE 805 SCD2 is a medical device that received FDA 510(k) clearance on 1987-07-28. The listed applicant is Phonic Ear, Inc.. The 510(k) number is K872474.

When did POST-AURICULAR HEARING AID MODEL PE 805 SCD2 receive FDA 510(k) clearance?

POST-AURICULAR HEARING AID MODEL PE 805 SCD2 received FDA 510(k) clearance on 1987-07-28, under 510(k) number K872474.

Who is the listed applicant for POST-AURICULAR HEARING AID MODEL PE 805 SCD2?

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

What is the FDA product code for POST-AURICULAR HEARING AID MODEL PE 805 SCD2?

The FDA product code for POST-AURICULAR HEARING AID MODEL PE 805 SCD2 is ESD.

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Other records listing Phonic 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.

K043090EASYLISTENER 2 FM, RADIUM FM AND VOCALIGHT INFRARED SOUND FIELD SYSTEMSK974658INFRARED GROUP AMPLIFICATION SYSTEM, INFRARED EMITTER, INFRARED BODY WORN RECEIVER, INFRARED HEADSET RECEIVER-STEREO, ITK974287FM RECEIVER - AUDITORY TRAINERK950730GROUP AUDITORY TRAINER (GROUP AMPLIFICATION SYSTEM)K940313PHONIC EARK923234PE 400IR, PE 400T, PE 400E

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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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