OTICON/LOGIC
K-Number: K950381 · 1995-02-27
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Device Summary
Frequently Asked Questions
What is the OTICON/LOGIC?
OTICON/LOGIC is a medical device that received FDA 510(k) clearance on 1995-02-27. The listed applicant is Oticon, Inc.. The 510(k) number is K950381.
When did OTICON/LOGIC receive FDA 510(k) clearance?
OTICON/LOGIC received FDA 510(k) clearance on 1995-02-27, under 510(k) number K950381.
Who is the listed applicant for OTICON/LOGIC?
The FDA 510(k) record lists Oticon, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OTICON/LOGIC?
The FDA product code for OTICON/LOGIC 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 Oticon, 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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