RADIOEAR M430 PP
K-Number: K841934 · 1984-09-07
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Device Summary
Frequently Asked Questions
What is the RADIOEAR M430 PP?
RADIOEAR M430 PP is a medical device that received FDA 510(k) clearance on 1984-09-07. The listed applicant is Radioear Corp.. The 510(k) number is K841934.
When did RADIOEAR M430 PP receive FDA 510(k) clearance?
RADIOEAR M430 PP received FDA 510(k) clearance on 1984-09-07, under 510(k) number K841934.
Who is the listed applicant for RADIOEAR M430 PP?
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 M430 PP?
The FDA product code for RADIOEAR M430 PP 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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