BEHIND-THE-EAR #123 AGCI
K-Number: K832326 · 1983-09-29
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Device Summary
Frequently Asked Questions
What is the BEHIND-THE-EAR #123 AGCI?
BEHIND-THE-EAR #123 AGCI is a medical device that received FDA 510(k) clearance on 1983-09-29. The listed applicant is Danavox, Inc.. The 510(k) number is K832326.
When did BEHIND-THE-EAR #123 AGCI receive FDA 510(k) clearance?
BEHIND-THE-EAR #123 AGCI received FDA 510(k) clearance on 1983-09-29, under 510(k) number K832326.
Who is the listed applicant for BEHIND-THE-EAR #123 AGCI?
The FDA 510(k) record lists Danavox, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BEHIND-THE-EAR #123 AGCI?
The FDA product code for BEHIND-THE-EAR #123 AGCI 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 Danavox, 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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