MAICO IN-THE-EAR MODEL RD-312 CIC
K-Number: K950637 · 1995-03-21
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Device Summary
Frequently Asked Questions
What is the MAICO IN-THE-EAR MODEL RD-312 CIC?
MAICO IN-THE-EAR MODEL RD-312 CIC is a medical device that received FDA 510(k) clearance on 1995-03-21. The listed applicant is Maico Hearing Instruments, Inc.. The 510(k) number is K950637.
When did MAICO IN-THE-EAR MODEL RD-312 CIC receive FDA 510(k) clearance?
MAICO IN-THE-EAR MODEL RD-312 CIC received FDA 510(k) clearance on 1995-03-21, under 510(k) number K950637.
Who is the listed applicant for MAICO IN-THE-EAR MODEL RD-312 CIC?
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 MAICO IN-THE-EAR MODEL RD-312 CIC?
The FDA product code for MAICO IN-THE-EAR MODEL RD-312 CIC 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.
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