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FDA 510(k)

321Q MINIMUM ENERGY TINNITUS SUPPRESSOR

K-Number: K922572 · 1992-11-02

ApplicantMicrobio-Medics, Inc.
Decision Date1992-11-02
Product CodeKLW
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

321Q MINIMUM ENERGY TINNITUS SUPPRESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Microbio-Medics, Inc.. It received FDA 510(k) clearance on 1992-11-02 under 510(k) number K922572. 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 321Q MINIMUM ENERGY TINNITUS SUPPRESSOR?

321Q MINIMUM ENERGY TINNITUS SUPPRESSOR is a medical device that received FDA 510(k) clearance on 1992-11-02. The listed applicant is Microbio-Medics, Inc.. The 510(k) number is K922572.

When did 321Q MINIMUM ENERGY TINNITUS SUPPRESSOR receive FDA 510(k) clearance?

321Q MINIMUM ENERGY TINNITUS SUPPRESSOR received FDA 510(k) clearance on 1992-11-02, under 510(k) number K922572.

Who is the listed applicant for 321Q MINIMUM ENERGY TINNITUS SUPPRESSOR?

The FDA 510(k) record lists Microbio-Medics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 321Q MINIMUM ENERGY TINNITUS SUPPRESSOR?

The FDA product code for 321Q MINIMUM ENERGY TINNITUS SUPPRESSOR is KLW.

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Related Devices (Code: KLW)

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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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