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FDA 510(k)

UNIVAR UNIVERSAL DENTIN VARNISH

K-Number: K852755 · 1985-09-23

Decision Date1985-09-23
Product CodeLBH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

UNIVAR UNIVERSAL DENTIN 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 1985-09-23 under 510(k) number K852755. 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 UNIVAR UNIVERSAL DENTIN VARNISH?

UNIVAR UNIVERSAL DENTIN VARNISH is a medical device that received FDA 510(k) clearance on 1985-09-23. The listed applicant is Scientific Pharmaceuticals, Inc.. The 510(k) number is K852755.

When did UNIVAR UNIVERSAL DENTIN VARNISH receive FDA 510(k) clearance?

UNIVAR UNIVERSAL DENTIN VARNISH received FDA 510(k) clearance on 1985-09-23, under 510(k) number K852755.

Who is the listed applicant for UNIVAR UNIVERSAL DENTIN 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 UNIVAR UNIVERSAL DENTIN VARNISH?

The FDA product code for UNIVAR UNIVERSAL DENTIN 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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