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FDA 510(k)

OTOSONIC ACS K

K-Number: K922827 · 1992-07-01

ApplicantBeltone Electronics Corp.
Decision Date1992-07-01
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

OTOSONIC ACS K is the device name listed in this FDA 510(k) record. The listed applicant is Beltone Electronics Corp.. It received FDA 510(k) clearance on 1992-07-01 under 510(k) number K922827. 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 OTOSONIC ACS K?

OTOSONIC ACS K is a medical device that received FDA 510(k) clearance on 1992-07-01. The listed applicant is Beltone Electronics Corp.. The 510(k) number is K922827.

When did OTOSONIC ACS K receive FDA 510(k) clearance?

OTOSONIC ACS K received FDA 510(k) clearance on 1992-07-01, under 510(k) number K922827.

Who is the listed applicant for OTOSONIC ACS K?

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

What is the FDA product code for OTOSONIC ACS K?

The FDA product code for OTOSONIC ACS K is ESD.

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Other records listing Beltone Electronics Corp. as applicant

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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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