Llis, Vittra APS
K-Number: K191306 · 2019-12-16
ApplicantDentscare Ltda
Decision Date2019-12-16
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Llis, Vittra APS is a medical device manufactured by Dentscare Ltda. It received FDA 510(k) clearance on 2019-12-16 under approval number K191306. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Llis, Vittra APS?
Llis, Vittra APS is a medical device that received FDA 510(k) clearance on 2019-12-16. It is manufactured by Dentscare Ltda. The 510(k) number is K191306.
When was Llis, Vittra APS approved by the FDA?
Llis, Vittra APS received FDA 510(k) clearance on 2019-12-16, under approval number K191306.
What company makes Llis, Vittra APS?
Llis, Vittra APS is manufactured by Dentscare Ltda.
What is the FDA product code for Llis, Vittra APS?
The FDA product code for Llis, Vittra APS is EBF.
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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.