BELTONE CONCERTO S
K-Number: K944502 · 1994-10-20
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Device Summary
Frequently Asked Questions
What is the BELTONE CONCERTO S?
BELTONE CONCERTO S is a medical device that received FDA 510(k) clearance on 1994-10-20. The listed applicant is Beltone Electronics Corp.. The 510(k) number is K944502.
When did BELTONE CONCERTO S receive FDA 510(k) clearance?
BELTONE CONCERTO S received FDA 510(k) clearance on 1994-10-20, under 510(k) number K944502.
Who is the listed applicant for BELTONE CONCERTO S?
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 CONCERTO S?
The FDA product code for BELTONE CONCERTO S 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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