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)

WIDEX MODEL SENSO DIGITAL (C9)

K-Number: K965254 · 1997-03-12

ApplicantWidex Hearing Aid Co., Inc.
Decision Date1997-03-12
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

WIDEX MODEL SENSO DIGITAL (C9) is the device name listed in this FDA 510(k) record. The listed applicant is Widex Hearing Aid Co., Inc.. It received FDA 510(k) clearance on 1997-03-12 under 510(k) number K965254. 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 WIDEX MODEL SENSO DIGITAL (C9)?

WIDEX MODEL SENSO DIGITAL (C9) is a medical device that received FDA 510(k) clearance on 1997-03-12. The listed applicant is Widex Hearing Aid Co., Inc.. The 510(k) number is K965254.

When did WIDEX MODEL SENSO DIGITAL (C9) receive FDA 510(k) clearance?

WIDEX MODEL SENSO DIGITAL (C9) received FDA 510(k) clearance on 1997-03-12, under 510(k) number K965254.

Who is the listed applicant for WIDEX MODEL SENSO DIGITAL (C9)?

The FDA 510(k) record lists Widex Hearing Aid Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WIDEX MODEL SENSO DIGITAL (C9)?

The FDA product code for WIDEX MODEL SENSO DIGITAL (C9) 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 Widex Hearing Aid Co., 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.

K080955ZEN PROGRAM (MIND 440 HEARING AID)K971535WIDEX SENSO DIGITAL (MINI CANAL)K970904WIDEX SENSO DIGITAL (CIC)K965218SENSO DIGITAL (C18)K955879WIDEX MODEL SENSO DIGITAL (C16)K955878WIDEX MODEL SENSO DIGITAL (C8)

View all 52 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.

↑