AUDIOTONE MODEL A-98
K-Number: K926091 · 1993-02-12
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Device Summary
Frequently Asked Questions
What is the AUDIOTONE MODEL A-98?
AUDIOTONE MODEL A-98 is a medical device that received FDA 510(k) clearance on 1993-02-12. The listed applicant is Miracle-Ear, Inc.. The 510(k) number is K926091.
When did AUDIOTONE MODEL A-98 receive FDA 510(k) clearance?
AUDIOTONE MODEL A-98 received FDA 510(k) clearance on 1993-02-12, under 510(k) number K926091.
Who is the listed applicant for AUDIOTONE MODEL A-98?
The FDA 510(k) record lists Miracle-Ear, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AUDIOTONE MODEL A-98?
The FDA product code for AUDIOTONE MODEL A-98 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 Miracle-Ear, 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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