ARGENCO Y (TYPE III/IV DENTAL ALLOY CROWN/BRIDGE
K-Number: K902665 · 1990-08-07
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Device Summary
Frequently Asked Questions
What is the ARGENCO Y (TYPE III/IV DENTAL ALLOY CROWN/BRIDGE?
ARGENCO Y (TYPE III/IV DENTAL ALLOY CROWN/BRIDGE is a medical device that received FDA 510(k) clearance on 1990-08-07. The listed applicant is Argen Precious Metals, Inc.. The 510(k) number is K902665.
When did ARGENCO Y (TYPE III/IV DENTAL ALLOY CROWN/BRIDGE receive FDA 510(k) clearance?
ARGENCO Y (TYPE III/IV DENTAL ALLOY CROWN/BRIDGE received FDA 510(k) clearance on 1990-08-07, under 510(k) number K902665.
Who is the listed applicant for ARGENCO Y (TYPE III/IV DENTAL ALLOY CROWN/BRIDGE?
The FDA 510(k) record lists Argen Precious Metals, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ARGENCO Y (TYPE III/IV DENTAL ALLOY CROWN/BRIDGE?
The FDA product code for ARGENCO Y (TYPE III/IV DENTAL ALLOY CROWN/BRIDGE is EJS.
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 Argen Precious Metals, 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: EJS)
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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