101M IN-THE-EAR
K-Number: K823073 · 1983-01-07
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Device Summary
Frequently Asked Questions
What is the 101M IN-THE-EAR?
101M IN-THE-EAR is a medical device that received FDA 510(k) clearance on 1983-01-07. The listed applicant is Danavox, Inc.. The 510(k) number is K823073.
When did 101M IN-THE-EAR receive FDA 510(k) clearance?
101M IN-THE-EAR received FDA 510(k) clearance on 1983-01-07, under 510(k) number K823073.
Who is the listed applicant for 101M IN-THE-EAR?
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 101M IN-THE-EAR?
The FDA product code for 101M IN-THE-EAR is ESD.
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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