WILL-CERAM W-3
K-Number: K771596 · 1977-08-26
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Device Summary
Frequently Asked Questions
What is the WILL-CERAM W-3?
WILL-CERAM W-3 is a medical device that received FDA 510(k) clearance on 1977-08-26. The listed applicant is Williams Gold Refining Co., Inc.. The 510(k) number is K771596.
When did WILL-CERAM W-3 receive FDA 510(k) clearance?
WILL-CERAM W-3 received FDA 510(k) clearance on 1977-08-26, under 510(k) number K771596.
Who is the listed applicant for WILL-CERAM W-3?
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 WILL-CERAM W-3?
The FDA product code for WILL-CERAM W-3 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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