VISION PROPHY PASTE WITHOUT FLUORIDE
K-Number: K933893 · 1993-11-16
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Device Summary
Frequently Asked Questions
What is the VISION PROPHY PASTE WITHOUT FLUORIDE?
VISION PROPHY PASTE WITHOUT FLUORIDE is a medical device that received FDA 510(k) clearance on 1993-11-16. The listed applicant is Block Drug Company, Inc.. The 510(k) number is K933893.
When did VISION PROPHY PASTE WITHOUT FLUORIDE receive FDA 510(k) clearance?
VISION PROPHY PASTE WITHOUT FLUORIDE received FDA 510(k) clearance on 1993-11-16, under 510(k) number K933893.
Who is the listed applicant for VISION PROPHY PASTE WITHOUT FLUORIDE?
The FDA 510(k) record lists Block Drug Company, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VISION PROPHY PASTE WITHOUT FLUORIDE?
The FDA product code for VISION PROPHY PASTE WITHOUT FLUORIDE is EJR.
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 Block Drug Company, 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: EJR)
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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