Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

RADIOEAR RE SERIES HEARING AIDS

K-Number: K781458 · 1978-09-07

ApplicantRadioear Corp.
Decision Date1978-09-07
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

RADIOEAR RE SERIES HEARING AIDS is the device name listed in this FDA 510(k) record. The listed applicant is Radioear Corp.. It received FDA 510(k) clearance on 1978-09-07 under 510(k) number K781458. 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 RADIOEAR RE SERIES HEARING AIDS?

RADIOEAR RE SERIES HEARING AIDS is a medical device that received FDA 510(k) clearance on 1978-09-07. The listed applicant is Radioear Corp.. The 510(k) number is K781458.

When did RADIOEAR RE SERIES HEARING AIDS receive FDA 510(k) clearance?

RADIOEAR RE SERIES HEARING AIDS received FDA 510(k) clearance on 1978-09-07, under 510(k) number K781458.

Who is the listed applicant for RADIOEAR RE SERIES HEARING AIDS?

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

What is the FDA product code for RADIOEAR RE SERIES HEARING AIDS?

The FDA product code for RADIOEAR RE SERIES HEARING AIDS 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 Radioear 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.

K841934RADIOEAR M430 PPK841933RADIOEAR M420HK841475HEARING AID MODEL M400K841474HEARING AID MODEL P500K841473HEARING AID MODEL 440PPCK834523MODEL M410D HEARING AID

View all 14 devices →

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.

↑