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FDA 510(k)

BTE HEARING AID PERSONIC 410

K-Number: K923490 · 1992-08-06

ApplicantOticon Corp.
Decision Date1992-08-06
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

BTE HEARING AID PERSONIC 410 is the device name listed in this FDA 510(k) record. The listed applicant is Oticon Corp.. It received FDA 510(k) clearance on 1992-08-06 under 510(k) number K923490. 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 BTE HEARING AID PERSONIC 410?

BTE HEARING AID PERSONIC 410 is a medical device that received FDA 510(k) clearance on 1992-08-06. The listed applicant is Oticon Corp.. The 510(k) number is K923490.

When did BTE HEARING AID PERSONIC 410 receive FDA 510(k) clearance?

BTE HEARING AID PERSONIC 410 received FDA 510(k) clearance on 1992-08-06, under 510(k) number K923490.

Who is the listed applicant for BTE HEARING AID PERSONIC 410?

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

What is the FDA product code for BTE HEARING AID PERSONIC 410?

The FDA product code for BTE HEARING AID PERSONIC 410 is ESD.

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Other records listing Oticon Corp. 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.

K963788PRIMOFOCUS COMPACTK932670OTICON MFK923491BTE HEARING AID PERSONIC 425K923388BTE HEARING AID OTICON MODEL: MULTIFOCUS POWERK905555A-ZILICONEK904673OTICAON BTE MODEL E34P

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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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