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FDA 510(k)

TINNITUS DEVICES

K-Number: K790064 · 1979-02-16

ApplicantVicon Instrument Co.
Decision Date1979-02-16
Product CodeETS
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

TINNITUS DEVICES is the device name listed in this FDA 510(k) record. The listed applicant is Vicon Instrument Co.. It received FDA 510(k) clearance on 1979-02-16 under 510(k) number K790064. The device is classified under product code ETS. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TINNITUS DEVICES?

TINNITUS DEVICES is a medical device that received FDA 510(k) clearance on 1979-02-16. The listed applicant is Vicon Instrument Co.. The 510(k) number is K790064.

When did TINNITUS DEVICES receive FDA 510(k) clearance?

TINNITUS DEVICES received FDA 510(k) clearance on 1979-02-16, under 510(k) number K790064.

Who is the listed applicant for TINNITUS DEVICES?

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

What is the FDA product code for TINNITUS DEVICES?

The FDA product code for TINNITUS DEVICES is ETS.

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.

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Other records listing Vicon Instrument Co. 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.

K811751FINETONE MODEL VI HEARING AIDK790878SCREENING AUDIOMETER, HIGH FREQUENCYK771769TINNITUS MASKERS, MODELS S564&S574K771762MODULAR HEARING DEVICE, MODEL S291K770938TINNITUS AID, MODEL S244K761216HEARING AIDS (MODEL E-552 S-712)

View all 8 devices →

Related Devices (Code: ETS)

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.

K813557AUDITORY STIMULATORWestern Advanced Technology, Inc.K811790OCTOTOXIC SCREENERWestern Advanced Technology, Inc.K811772AUDITORY LOCALIZERWestern Advanced Technology, Inc.K771188REVERSING CLICK GENERATOR RCG6Teca, 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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