RADIOEAR MODEL 2080 (HEARING AID)
K-Number: K800332 · 1980-03-05
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Device Summary
Frequently Asked Questions
What is the RADIOEAR MODEL 2080 (HEARING AID)?
RADIOEAR MODEL 2080 (HEARING AID) is a medical device that received FDA 510(k) clearance on 1980-03-05. The listed applicant is Radioear Corp.. The 510(k) number is K800332.
When did RADIOEAR MODEL 2080 (HEARING AID) receive FDA 510(k) clearance?
RADIOEAR MODEL 2080 (HEARING AID) received FDA 510(k) clearance on 1980-03-05, under 510(k) number K800332.
Who is the listed applicant for RADIOEAR MODEL 2080 (HEARING AID)?
The FDA 510(k) record lists Radioear Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RADIOEAR MODEL 2080 (HEARING AID)?
The FDA product code for RADIOEAR MODEL 2080 (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 Radioear 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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