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FDA 510(k)

VLC GLASS IONOMER LINER

K-Number: K911244 · 1991-06-28

ApplicantDentsply Intl.
Decision Date1991-06-28
Product CodeEJK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VLC GLASS IONOMER LINER is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Intl.. It received FDA 510(k) clearance on 1991-06-28 under 510(k) number K911244. The device is classified under product code EJK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VLC GLASS IONOMER LINER?

VLC GLASS IONOMER LINER is a medical device that received FDA 510(k) clearance on 1991-06-28. The listed applicant is Dentsply Intl.. The 510(k) number is K911244.

When did VLC GLASS IONOMER LINER receive FDA 510(k) clearance?

VLC GLASS IONOMER LINER received FDA 510(k) clearance on 1991-06-28, under 510(k) number K911244.

Who is the listed applicant for VLC GLASS IONOMER LINER?

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 VLC GLASS IONOMER LINER?

The FDA product code for VLC GLASS IONOMER LINER is EJK.

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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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