MODIFIED HEARING AID (IN-THE-EAR)
K-Number: K902487 · 1990-10-09
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Device Summary
Frequently Asked Questions
What is the MODIFIED HEARING AID (IN-THE-EAR)?
MODIFIED HEARING AID (IN-THE-EAR) is a medical device that received FDA 510(k) clearance on 1990-10-09. The listed applicant is Audio Hearing Aid Service. The 510(k) number is K902487.
When did MODIFIED HEARING AID (IN-THE-EAR) receive FDA 510(k) clearance?
MODIFIED HEARING AID (IN-THE-EAR) received FDA 510(k) clearance on 1990-10-09, under 510(k) number K902487.
Who is the listed applicant for MODIFIED HEARING AID (IN-THE-EAR)?
The FDA 510(k) record lists Audio Hearing Aid Service as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODIFIED HEARING AID (IN-THE-EAR)?
The FDA product code for MODIFIED HEARING AID (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.
Other records listing Audio Hearing Aid Service 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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