PERSONAL AMPLIFIER
K-Number: K832168 · 1983-11-21
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Device Summary
Frequently Asked Questions
What is the PERSONAL AMPLIFIER?
PERSONAL AMPLIFIER is a medical device that received FDA 510(k) clearance on 1983-11-21. The listed applicant is Electone, Inc.. The 510(k) number is K832168.
When did PERSONAL AMPLIFIER receive FDA 510(k) clearance?
PERSONAL AMPLIFIER received FDA 510(k) clearance on 1983-11-21, under 510(k) number K832168.
Who is the listed applicant for PERSONAL AMPLIFIER?
The FDA 510(k) record lists Electone, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PERSONAL AMPLIFIER?
The FDA product code for PERSONAL AMPLIFIER 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 Electone, Inc. 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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