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FDA 510(k)

CAVITY VARNISH

K-Number: K810913 · 1981-09-21

ApplicantDentsply Intl.
Decision Date1981-09-21
Product CodeLBH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CAVITY VARNISH is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1981-09-21 under 510(k) number K810913. 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 CAVITY VARNISH?

CAVITY VARNISH is a medical device that received FDA 510(k) clearance on 1981-09-21. The listed applicant is Dentsply Intl.. The 510(k) number is K810913.

When did CAVITY VARNISH receive FDA 510(k) clearance?

CAVITY VARNISH received FDA 510(k) clearance on 1981-09-21, under 510(k) number K810913.

Who is the listed applicant for CAVITY VARNISH?

The FDA 510(k) record lists Dentsply Intl. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CAVITY VARNISH?

The FDA product code for CAVITY VARNISH is LBH.

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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.

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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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