PROPHY PASTE
K-Number: K771401 · 1977-08-22
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Device Summary
Frequently Asked Questions
What is the PROPHY PASTE?
PROPHY PASTE is a medical device that received FDA 510(k) clearance on 1977-08-22. The listed applicant is L.D. Caulk Co.. The 510(k) number is K771401.
When did PROPHY PASTE receive FDA 510(k) clearance?
PROPHY PASTE received FDA 510(k) clearance on 1977-08-22, under 510(k) number K771401.
Who is the listed applicant for PROPHY PASTE?
The FDA 510(k) record lists L.D. Caulk Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PROPHY PASTE?
The FDA product code for PROPHY PASTE 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 L.D. Caulk 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: 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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