ARGEDENT 88, DENTAL ALLOY FOR PORCELAIN)
K-Number: K891600 · 1989-06-14
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Device Summary
Frequently Asked Questions
What is the ARGEDENT 88, DENTAL ALLOY FOR PORCELAIN)?
ARGEDENT 88, DENTAL ALLOY FOR PORCELAIN) is a medical device that received FDA 510(k) clearance on 1989-06-14. The listed applicant is Argen Precious Metals, Inc.. The 510(k) number is K891600.
When did ARGEDENT 88, DENTAL ALLOY FOR PORCELAIN) receive FDA 510(k) clearance?
ARGEDENT 88, DENTAL ALLOY FOR PORCELAIN) received FDA 510(k) clearance on 1989-06-14, under 510(k) number K891600.
Who is the listed applicant for ARGEDENT 88, DENTAL ALLOY FOR PORCELAIN)?
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 ARGEDENT 88, DENTAL ALLOY FOR PORCELAIN)?
The FDA product code for ARGEDENT 88, DENTAL ALLOY FOR PORCELAIN) is EJT.
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: EJT)
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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