MICRO-EAR CANAL IN-THE-EAR HEARING AID
K-Number: K870079 · 1987-03-03
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Device Summary
Frequently Asked Questions
What is the MICRO-EAR CANAL IN-THE-EAR HEARING AID?
MICRO-EAR CANAL IN-THE-EAR HEARING AID is a medical device that received FDA 510(k) clearance on 1987-03-03. The listed applicant is Micro-Ear Hearing Center, Inc.. The 510(k) number is K870079.
When did MICRO-EAR CANAL IN-THE-EAR HEARING AID receive FDA 510(k) clearance?
MICRO-EAR CANAL IN-THE-EAR HEARING AID received FDA 510(k) clearance on 1987-03-03, under 510(k) number K870079.
Who is the listed applicant for MICRO-EAR CANAL IN-THE-EAR HEARING AID?
The FDA 510(k) record lists Micro-Ear Hearing Center, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MICRO-EAR CANAL IN-THE-EAR HEARING AID?
The FDA product code for MICRO-EAR CANAL IN-THE-EAR HEARING AID 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 Micro-Ear Hearing Center, 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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