HEARING AID (ALL-IN-THE-EAR)
K-Number: K912399 · 1992-03-12
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Device Summary
Frequently Asked Questions
What is the HEARING AID (ALL-IN-THE-EAR)?
HEARING AID (ALL-IN-THE-EAR) is a medical device that received FDA 510(k) clearance on 1992-03-12. The listed applicant is Carlson'S Heritage Hearing Aid Center. The 510(k) number is K912399.
When did HEARING AID (ALL-IN-THE-EAR) receive FDA 510(k) clearance?
HEARING AID (ALL-IN-THE-EAR) received FDA 510(k) clearance on 1992-03-12, under 510(k) number K912399.
Who is the listed applicant for HEARING AID (ALL-IN-THE-EAR)?
The FDA 510(k) record lists Carlson'S Heritage Hearing Aid Center as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HEARING AID (ALL-IN-THE-EAR)?
The FDA product code for HEARING AID (ALL-IN-THE-EAR) 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.
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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