SPARTAN -ALLOY FOR PORCELAIN FUSED TO METAL
K-Number: K850699 · 1985-03-18
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Device Summary
Frequently Asked Questions
What is the SPARTAN -ALLOY FOR PORCELAIN FUSED TO METAL?
SPARTAN -ALLOY FOR PORCELAIN FUSED TO METAL is a medical device that received FDA 510(k) clearance on 1985-03-18. The listed applicant is Williams Gold Refining Co., Inc.. The 510(k) number is K850699.
When did SPARTAN -ALLOY FOR PORCELAIN FUSED TO METAL receive FDA 510(k) clearance?
SPARTAN -ALLOY FOR PORCELAIN FUSED TO METAL received FDA 510(k) clearance on 1985-03-18, under 510(k) number K850699.
Who is the listed applicant for SPARTAN -ALLOY FOR PORCELAIN FUSED TO METAL?
The FDA 510(k) record lists Williams Gold Refining Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SPARTAN -ALLOY FOR PORCELAIN FUSED TO METAL?
The FDA product code for SPARTAN -ALLOY FOR PORCELAIN FUSED TO METAL 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 Williams Gold Refining Co., 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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