BOSCH TOP STAR III
K-Number: K820041 · 1982-01-22
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Device Summary
Frequently Asked Questions
What is the BOSCH TOP STAR III?
BOSCH TOP STAR III is a medical device that received FDA 510(k) clearance on 1982-01-22. The listed applicant is Bosch Hearing Instruments, Inc.. The 510(k) number is K820041.
When did BOSCH TOP STAR III receive FDA 510(k) clearance?
BOSCH TOP STAR III received FDA 510(k) clearance on 1982-01-22, under 510(k) number K820041.
Who is the listed applicant for BOSCH TOP STAR III?
The FDA 510(k) record lists Bosch Hearing Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BOSCH TOP STAR III?
The FDA product code for BOSCH TOP STAR III 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 Bosch 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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