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FDA 510(k)

RESOUND CUSTOM IN-THE CANAL HEARING AID PHS-3

K-Number: K893927 · 1989-08-04

ApplicantResound Corp.
Decision Date1989-08-04
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

RESOUND CUSTOM IN-THE CANAL HEARING AID PHS-3 is the device name listed in this FDA 510(k) record. The listed applicant is Resound Corp.. It received FDA 510(k) clearance on 1989-08-04 under 510(k) number K893927. 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 RESOUND CUSTOM IN-THE CANAL HEARING AID PHS-3?

RESOUND CUSTOM IN-THE CANAL HEARING AID PHS-3 is a medical device that received FDA 510(k) clearance on 1989-08-04. The listed applicant is Resound Corp.. The 510(k) number is K893927.

When did RESOUND CUSTOM IN-THE CANAL HEARING AID PHS-3 receive FDA 510(k) clearance?

RESOUND CUSTOM IN-THE CANAL HEARING AID PHS-3 received FDA 510(k) clearance on 1989-08-04, under 510(k) number K893927.

Who is the listed applicant for RESOUND CUSTOM IN-THE CANAL HEARING AID PHS-3?

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

What is the FDA product code for RESOUND CUSTOM IN-THE CANAL HEARING AID PHS-3?

The FDA product code for RESOUND CUSTOM IN-THE CANAL HEARING AID PHS-3 is ESD.

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Other records listing Resound 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.

K984547DIGITAL LGOB PROCEDURE USING RESOUND, DIGITAL 5000 SERIES HEARING AIDSK974081RESOUND STEALTH CICK974257RESOUND DIGITAL 2000-BT W/DIGITAL 2000-DF (DIGITAL PROGRAMMER)K971605RESOUND ED4 PERSONAL HEARING SYSTEM W/REMOTE CONTROL OPTIONK970215AUDALLION II HEARING SYSTEMK964557RESOUND BT4 PERSONAL HEARING SYSTEM W/REMOTE CONTROL OPTION

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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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