OTICON MODEL E19VF EARETTE HEARING AID
K-Number: K800316 · 1980-02-26
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Device Summary
Frequently Asked Questions
What is the OTICON MODEL E19VF EARETTE HEARING AID?
OTICON MODEL E19VF EARETTE HEARING AID is a medical device that received FDA 510(k) clearance on 1980-02-26. The listed applicant is Oticon Corp.. The 510(k) number is K800316.
When did OTICON MODEL E19VF EARETTE HEARING AID receive FDA 510(k) clearance?
OTICON MODEL E19VF EARETTE HEARING AID received FDA 510(k) clearance on 1980-02-26, under 510(k) number K800316.
Who is the listed applicant for OTICON MODEL E19VF EARETTE HEARING AID?
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 OTICON MODEL E19VF EARETTE HEARING AID?
The FDA product code for OTICON MODEL E19VF EARETTE HEARING AID 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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