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)

TINNITUS MASKERS MODEL S584

K-Number: K790190 · 1979-02-12

ApplicantVican Instrument Co.
Decision Date1979-02-12
Product CodeKLW
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

TINNITUS MASKERS MODEL S584 is the device name listed in this FDA 510(k) record. The listed applicant is Vican Instrument Co.. It received FDA 510(k) clearance on 1979-02-12 under 510(k) number K790190. The device is classified under product code KLW. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TINNITUS MASKERS MODEL S584?

TINNITUS MASKERS MODEL S584 is a medical device that received FDA 510(k) clearance on 1979-02-12. The listed applicant is Vican Instrument Co.. The 510(k) number is K790190.

When did TINNITUS MASKERS MODEL S584 receive FDA 510(k) clearance?

TINNITUS MASKERS MODEL S584 received FDA 510(k) clearance on 1979-02-12, under 510(k) number K790190.

Who is the listed applicant for TINNITUS MASKERS MODEL S584?

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

What is the FDA product code for TINNITUS MASKERS MODEL S584?

The FDA product code for TINNITUS MASKERS MODEL S584 is KLW.

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

Related Devices (Code: KLW)

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.

K260413Levo Gen 2 Tinnitus Therapy SystemLevo Medical CorporationK260614Tinnitus TherapySivantos GmbHK233435Peace N Quiet (0.7.0)Pnq HealthK223694Tinearity G1 (6103); Tinearity G1 Adapters x3 (6042)Duearity ABK221168Tinnitogram Signal GeneratorGoldenear Company, Inc.K221125SilentCloudAureliym GmbH

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.

↑