HEARING AID, OTICON I II H
K-Number: K790301 · 1979-02-26
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Device Summary
Frequently Asked Questions
What is the HEARING AID, OTICON I II H?
HEARING AID, OTICON I II H is a medical device that received FDA 510(k) clearance on 1979-02-26. The listed applicant is Oticon Corp.. The 510(k) number is K790301.
When did HEARING AID, OTICON I II H receive FDA 510(k) clearance?
HEARING AID, OTICON I II H received FDA 510(k) clearance on 1979-02-26, under 510(k) number K790301.
Who is the listed applicant for HEARING AID, OTICON I II H?
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 HEARING AID, OTICON I II H?
The FDA product code for HEARING AID, OTICON I II H 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.
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
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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