OTICON DIGISOUND COMPACT
K-Number: K973886 · 1997-11-04
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Device Summary
Frequently Asked Questions
What is the OTICON DIGISOUND COMPACT?
OTICON DIGISOUND COMPACT is a medical device that received FDA 510(k) clearance on 1997-11-04. The listed applicant is Oticon, Inc.. The 510(k) number is K973886.
When did OTICON DIGISOUND COMPACT receive FDA 510(k) clearance?
OTICON DIGISOUND COMPACT received FDA 510(k) clearance on 1997-11-04, under 510(k) number K973886.
Who is the listed applicant for OTICON DIGISOUND COMPACT?
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 DIGISOUND COMPACT?
The FDA product code for OTICON DIGISOUND COMPACT 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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