SERIES MR IN-THE-EAR CUSTOM HEARING AID
K-Number: K840825 · 1984-03-30
Advertisement
Device Summary
Frequently Asked Questions
What is the SERIES MR IN-THE-EAR CUSTOM HEARING AID?
SERIES MR IN-THE-EAR CUSTOM HEARING AID is a medical device that received FDA 510(k) clearance on 1984-03-30. The listed applicant is Maico Hearing Instruments, Inc.. The 510(k) number is K840825.
When did SERIES MR IN-THE-EAR CUSTOM HEARING AID receive FDA 510(k) clearance?
SERIES MR IN-THE-EAR CUSTOM HEARING AID received FDA 510(k) clearance on 1984-03-30, under 510(k) number K840825.
Who is the listed applicant for SERIES MR IN-THE-EAR CUSTOM HEARING AID?
The FDA 510(k) record lists Maico Hearing Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SERIES MR IN-THE-EAR CUSTOM HEARING AID?
The FDA product code for SERIES MR IN-THE-EAR CUSTOM 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 Maico Hearing Instruments, 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.
Advertisement