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FDA 510(k)

HEARING AID(ALL IN EAR)

K-Number: K852244 · 1985-11-07

ApplicantOlympia Instruments, Inc.
Decision Date1985-11-07
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

HEARING AID(ALL IN EAR) is the device name listed in this FDA 510(k) record. The listed applicant is Olympia Instruments, Inc.. It received FDA 510(k) clearance on 1985-11-07 under 510(k) number K852244. 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 HEARING AID(ALL IN EAR)?

HEARING AID(ALL IN EAR) is a medical device that received FDA 510(k) clearance on 1985-11-07. The listed applicant is Olympia Instruments, Inc.. The 510(k) number is K852244.

When did HEARING AID(ALL IN EAR) receive FDA 510(k) clearance?

HEARING AID(ALL IN EAR) received FDA 510(k) clearance on 1985-11-07, under 510(k) number K852244.

Who is the listed applicant for HEARING AID(ALL IN EAR)?

The FDA 510(k) record lists Olympia Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEARING AID(ALL IN EAR)?

The FDA product code for HEARING AID(ALL IN EAR) is ESD.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Olympia Instruments, Inc. 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.

K896304OLYMPIA FACEPLATE MODULE

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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