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)

BELTONE OPTIMA 2000 CLEARVOICE SERIES, IN-THE-EAR

K-Number: K930310 · 1993-03-01

ApplicantBeltone Electronics Corp.
Decision Date1993-03-01
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

BELTONE OPTIMA 2000 CLEARVOICE SERIES, IN-THE-EAR is the device name listed in this FDA 510(k) record. The listed applicant is Beltone Electronics Corp.. It received FDA 510(k) clearance on 1993-03-01 under 510(k) number K930310. 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 BELTONE OPTIMA 2000 CLEARVOICE SERIES, IN-THE-EAR?

BELTONE OPTIMA 2000 CLEARVOICE SERIES, IN-THE-EAR is a medical device that received FDA 510(k) clearance on 1993-03-01. The listed applicant is Beltone Electronics Corp.. The 510(k) number is K930310.

When did BELTONE OPTIMA 2000 CLEARVOICE SERIES, IN-THE-EAR receive FDA 510(k) clearance?

BELTONE OPTIMA 2000 CLEARVOICE SERIES, IN-THE-EAR received FDA 510(k) clearance on 1993-03-01, under 510(k) number K930310.

Who is the listed applicant for BELTONE OPTIMA 2000 CLEARVOICE SERIES, IN-THE-EAR?

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

What is the FDA product code for BELTONE OPTIMA 2000 CLEARVOICE SERIES, IN-THE-EAR?

The FDA product code for BELTONE OPTIMA 2000 CLEARVOICE SERIES, IN-THE-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 Beltone Electronics 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.

K971852AIR CONDUCTION HAEARING AIDSK963958IMPRESS, PERFECTA, ACU-FORM, AND ACUFITK955930BELTONE COMPOSER 2000 BTE HPK954936BELTONE ULTIMA 80 OTOSONIC POWER PASK943616BELTONE PERSONAL HEARING SCREENERK951587BELTONE PETITE PLUS BELTONE PETITE PLUS CLEARVIOCE K

View all 42 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.

↑