BELTONE COMPOSER 2000 BTE HP
K-Number: K955930 · 1996-03-01
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Device Summary
Frequently Asked Questions
What is the BELTONE COMPOSER 2000 BTE HP?
BELTONE COMPOSER 2000 BTE HP is a medical device that received FDA 510(k) clearance on 1996-03-01. The listed applicant is Beltone Electronics Corp.. The 510(k) number is K955930.
When did BELTONE COMPOSER 2000 BTE HP receive FDA 510(k) clearance?
BELTONE COMPOSER 2000 BTE HP received FDA 510(k) clearance on 1996-03-01, under 510(k) number K955930.
Who is the listed applicant for BELTONE COMPOSER 2000 BTE HP?
The FDA 510(k) record lists Beltone Electronics Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BELTONE COMPOSER 2000 BTE HP?
The FDA product code for BELTONE COMPOSER 2000 BTE HP 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 Beltone Electronics Corp. 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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