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FDA 510(k)

SCI-PHARM UNIVERSAL CAVITY VARNISH

K-Number: K802926 · 1980-12-19

Decision Date1980-12-19
Product CodeLBH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SCI-PHARM UNIVERSAL CAVITY VARNISH is the device name listed in this FDA 510(k) record. The listed applicant is Scientific Pharmaceuticals, Inc.. It received FDA 510(k) clearance on 1980-12-19 under 510(k) number K802926. The device is classified under product code LBH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 72 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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