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FDA 510(k)

OUTPUT COMPRESSION LIMITER WITH ACTIVE TONE CONTROL

K-Number: K952452 · 1995-07-06

ApplicantArgosy Electronics
Decision Date1995-07-06
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

OUTPUT COMPRESSION LIMITER WITH ACTIVE TONE CONTROL is the device name listed in this FDA 510(k) record. The listed applicant is Argosy Electronics. It received FDA 510(k) clearance on 1995-07-06 under 510(k) number K952452. 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 OUTPUT COMPRESSION LIMITER WITH ACTIVE TONE CONTROL?

OUTPUT COMPRESSION LIMITER WITH ACTIVE TONE CONTROL is a medical device that received FDA 510(k) clearance on 1995-07-06. The listed applicant is Argosy Electronics. The 510(k) number is K952452.

When did OUTPUT COMPRESSION LIMITER WITH ACTIVE TONE CONTROL receive FDA 510(k) clearance?

OUTPUT COMPRESSION LIMITER WITH ACTIVE TONE CONTROL received FDA 510(k) clearance on 1995-07-06, under 510(k) number K952452.

Who is the listed applicant for OUTPUT COMPRESSION LIMITER WITH ACTIVE TONE CONTROL?

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

What is the FDA product code for OUTPUT COMPRESSION LIMITER WITH ACTIVE TONE CONTROL?

The FDA product code for OUTPUT COMPRESSION LIMITER WITH ACTIVE TONE CONTROL is ESD.

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Other records listing Argosy Electronics 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.

K974242ARGOSY PROGRAMMABLE ONQUEK971699ARGOSY DYNAMEQK961729ARGOSY PROGRAMMABLEK954038K-AMP 16, HI-BAND K-AMP, ULTRA COMPRESSION & HEARING PROTECTION/HEARING INSTRUMENTK952450WIDE DYNAMIC RANGE COMPRESSION WITH ACTIVE TONE CONTROLK952451CLASS D LINEAR WITH ACTIVE TONE CONTROL

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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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