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FDA 510(k)

ADAPTIVE COMPRESSION - CLASS D/ CLASS D AGCI

K-Number: K970430 · 1997-03-11

ApplicantMidwest City Hearing Aid Center
Decision Date1997-03-11
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ADAPTIVE COMPRESSION - CLASS D/ CLASS D AGCI is the device name listed in this FDA 510(k) record. The listed applicant is Midwest City Hearing Aid Center. It received FDA 510(k) clearance on 1997-03-11 under 510(k) number K970430. 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 ADAPTIVE COMPRESSION - CLASS D/ CLASS D AGCI?

ADAPTIVE COMPRESSION - CLASS D/ CLASS D AGCI is a medical device that received FDA 510(k) clearance on 1997-03-11. The listed applicant is Midwest City Hearing Aid Center. The 510(k) number is K970430.

When did ADAPTIVE COMPRESSION - CLASS D/ CLASS D AGCI receive FDA 510(k) clearance?

ADAPTIVE COMPRESSION - CLASS D/ CLASS D AGCI received FDA 510(k) clearance on 1997-03-11, under 510(k) number K970430.

Who is the listed applicant for ADAPTIVE COMPRESSION - CLASS D/ CLASS D AGCI?

The FDA 510(k) record lists Midwest City Hearing Aid Center as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ADAPTIVE COMPRESSION - CLASS D/ CLASS D AGCI?

The FDA product code for ADAPTIVE COMPRESSION - CLASS D/ CLASS D AGCI is ESD.

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Other records listing Midwest City Hearing Aid Center 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.

K963604DYNAMIC EQ II - 2 CHANNEL WIDE DYNAMIC RANGE COMPRESSIONK963607HORIZON 1 AND 2 PROGRAMABLE FULL SHELL AND IN THE CANALK953728RX12 LINEAR FULL SHELL AND IN THE CANALK953729K AMP FULL SHELL AND IN THE EARK953631SNIP INPUT COMPRESSION CLASS AK952986SPI-SECRET PERSONAL INSTRUMENT CIC

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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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