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FDA 510(k)

EARETTE HEARING AID OTICON #E25F

K-Number: K810986 · 1981-05-05

ApplicantOticon Corp.
Decision Date1981-05-05
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

EARETTE HEARING AID OTICON #E25F is the device name listed in this FDA 510(k) record. The listed applicant is Oticon Corp.. It received FDA 510(k) clearance on 1981-05-05 under 510(k) number K810986. 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 EARETTE HEARING AID OTICON #E25F?

EARETTE HEARING AID OTICON #E25F is a medical device that received FDA 510(k) clearance on 1981-05-05. The listed applicant is Oticon Corp.. The 510(k) number is K810986.

When did EARETTE HEARING AID OTICON #E25F receive FDA 510(k) clearance?

EARETTE HEARING AID OTICON #E25F received FDA 510(k) clearance on 1981-05-05, under 510(k) number K810986.

Who is the listed applicant for EARETTE HEARING AID OTICON #E25F?

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

What is the FDA product code for EARETTE HEARING AID OTICON #E25F?

The FDA product code for EARETTE HEARING AID OTICON #E25F 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 Oticon Corp. 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.

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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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