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FDA 510(k)

THE BELTONE AUDIO SCOUT

K-Number: K915323 · 1992-05-11

ApplicantBeltone Electronics Corp.
Decision Date1992-05-11
Product CodeEWO
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

THE BELTONE AUDIO SCOUT 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 1992-05-11 under 510(k) number K915323. The device is classified under product code EWO. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE BELTONE AUDIO SCOUT?

THE BELTONE AUDIO SCOUT is a medical device that received FDA 510(k) clearance on 1992-05-11. The listed applicant is Beltone Electronics Corp.. The 510(k) number is K915323.

When did THE BELTONE AUDIO SCOUT receive FDA 510(k) clearance?

THE BELTONE AUDIO SCOUT received FDA 510(k) clearance on 1992-05-11, under 510(k) number K915323.

Who is the listed applicant for THE BELTONE AUDIO SCOUT?

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 THE BELTONE AUDIO SCOUT?

The FDA product code for THE BELTONE AUDIO SCOUT is EWO.

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Other records listing Beltone Electronics Corp. as applicant

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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

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Related Devices (Code: EWO)

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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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