RADIOEAR MODEL RM-L & RM-C HEARING AID
K-Number: K800567 · 1980-04-29
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Device Summary
Frequently Asked Questions
What is the RADIOEAR MODEL RM-L & RM-C HEARING AID?
RADIOEAR MODEL RM-L & RM-C HEARING AID is a medical device that received FDA 510(k) clearance on 1980-04-29. The listed applicant is Radioear Corp.. The 510(k) number is K800567.
When did RADIOEAR MODEL RM-L & RM-C HEARING AID receive FDA 510(k) clearance?
RADIOEAR MODEL RM-L & RM-C HEARING AID received FDA 510(k) clearance on 1980-04-29, under 510(k) number K800567.
Who is the listed applicant for RADIOEAR MODEL RM-L & RM-C 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 RM-L & RM-C HEARING AID?
The FDA product code for RADIOEAR MODEL RM-L & RM-C 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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