DENSCO PROPHY PASTE
K-Number: K854829 · 1986-03-25
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Device Summary
Frequently Asked Questions
What is the DENSCO PROPHY PASTE?
DENSCO PROPHY PASTE is a medical device that received FDA 510(k) clearance on 1986-03-25. The listed applicant is Scientific Pharmaceuticals, Inc.. The 510(k) number is K854829.
When did DENSCO PROPHY PASTE receive FDA 510(k) clearance?
DENSCO PROPHY PASTE received FDA 510(k) clearance on 1986-03-25, under 510(k) number K854829.
Who is the listed applicant for DENSCO PROPHY PASTE?
The FDA 510(k) record lists Scientific Pharmaceuticals, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DENSCO PROPHY PASTE?
The FDA product code for DENSCO 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 Scientific Pharmaceuticals, 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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