SCI-PHARM UNIVERSAL CAVITY VARNISH
K-Number: K802926 · 1980-12-19
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Device Summary
Frequently Asked Questions
What is the SCI-PHARM UNIVERSAL CAVITY VARNISH?
SCI-PHARM UNIVERSAL CAVITY VARNISH is a medical device that received FDA 510(k) clearance on 1980-12-19. The listed applicant is Scientific Pharmaceuticals, Inc.. The 510(k) number is K802926.
When did SCI-PHARM UNIVERSAL CAVITY VARNISH receive FDA 510(k) clearance?
SCI-PHARM UNIVERSAL CAVITY VARNISH received FDA 510(k) clearance on 1980-12-19, under 510(k) number K802926.
Who is the listed applicant for SCI-PHARM UNIVERSAL CAVITY VARNISH?
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 SCI-PHARM UNIVERSAL CAVITY VARNISH?
The FDA product code for SCI-PHARM UNIVERSAL CAVITY VARNISH is LBH.
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: LBH)
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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