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FDA 510(k)

SONOTONE BEHIND THE EAR MODEL ST 45G

K-Number: K914899 · 1992-01-09

Decision Date1992-01-09
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

SONOTONE BEHIND THE EAR MODEL ST 45G is the device name listed in this FDA 510(k) record. The listed applicant is Sonotone Hearing Instruments. It received FDA 510(k) clearance on 1992-01-09 under 510(k) number K914899. 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 SONOTONE BEHIND THE EAR MODEL ST 45G?

SONOTONE BEHIND THE EAR MODEL ST 45G is a medical device that received FDA 510(k) clearance on 1992-01-09. The listed applicant is Sonotone Hearing Instruments. The 510(k) number is K914899.

When did SONOTONE BEHIND THE EAR MODEL ST 45G receive FDA 510(k) clearance?

SONOTONE BEHIND THE EAR MODEL ST 45G received FDA 510(k) clearance on 1992-01-09, under 510(k) number K914899.

Who is the listed applicant for SONOTONE BEHIND THE EAR MODEL ST 45G?

The FDA 510(k) record lists Sonotone Hearing Instruments as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SONOTONE BEHIND THE EAR MODEL ST 45G?

The FDA product code for SONOTONE BEHIND THE EAR MODEL ST 45G 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.

Other records listing Sonotone Hearing Instruments 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.

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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