CREDENT RADIOPAQUE CROWN & BRIDE
K-Number: K842476 · 1984-12-03
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Device Summary
Frequently Asked Questions
What is the CREDENT RADIOPAQUE CROWN & BRIDE?
CREDENT RADIOPAQUE CROWN & BRIDE is a medical device that received FDA 510(k) clearance on 1984-12-03. The listed applicant is Credent Co.. The 510(k) number is K842476.
When did CREDENT RADIOPAQUE CROWN & BRIDE receive FDA 510(k) clearance?
CREDENT RADIOPAQUE CROWN & BRIDE received FDA 510(k) clearance on 1984-12-03, under 510(k) number K842476.
Who is the listed applicant for CREDENT RADIOPAQUE CROWN & BRIDE?
The FDA 510(k) record lists Credent Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CREDENT RADIOPAQUE CROWN & BRIDE?
The FDA product code for CREDENT RADIOPAQUE CROWN & BRIDE is EBI.
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 Credent Co. 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: EBI)
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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