PORCELAIN VENEER SYSTEM LABORATORY KIT
K-Number: K852743 · 1985-07-31
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Device Summary
Frequently Asked Questions
What is the PORCELAIN VENEER SYSTEM LABORATORY KIT?
PORCELAIN VENEER SYSTEM LABORATORY KIT is a medical device that received FDA 510(k) clearance on 1985-07-31. The listed applicant is The S. S. White Co.. The 510(k) number is K852743.
When did PORCELAIN VENEER SYSTEM LABORATORY KIT receive FDA 510(k) clearance?
PORCELAIN VENEER SYSTEM LABORATORY KIT received FDA 510(k) clearance on 1985-07-31, under 510(k) number K852743.
Who is the listed applicant for PORCELAIN VENEER SYSTEM LABORATORY KIT?
The FDA 510(k) record lists The S. S. White Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PORCELAIN VENEER SYSTEM LABORATORY KIT?
The FDA product code for PORCELAIN VENEER SYSTEM LABORATORY KIT is EIH.
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 The S. S. White 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: EIH)
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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