AUDIO-ADI, AA SERIES
K-Number: K820993 · 1982-05-05
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Device Summary
Frequently Asked Questions
What is the AUDIO-ADI, AA SERIES?
AUDIO-ADI, AA SERIES is a medical device that received FDA 510(k) clearance on 1982-05-05. The listed applicant is Audio-Aid, Inc.. The 510(k) number is K820993.
When did AUDIO-ADI, AA SERIES receive FDA 510(k) clearance?
AUDIO-ADI, AA SERIES received FDA 510(k) clearance on 1982-05-05, under 510(k) number K820993.
Who is the listed applicant for AUDIO-ADI, AA SERIES?
The FDA 510(k) record lists Audio-Aid, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AUDIO-ADI, AA SERIES?
The FDA product code for AUDIO-ADI, AA SERIES 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 Audio-Aid, 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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