DiaPaste
K-Number: K210333 · 2021-03-25
ApplicantDiaDent Group International
Decision Date2021-03-25
Product CodeKIF
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
DiaPaste is a medical device manufactured by DiaDent Group International. It received FDA 510(k) clearance on 2021-03-25 under approval number K210333. The device is classified under product code KIF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the DiaPaste?
DiaPaste is a medical device that received FDA 510(k) clearance on 2021-03-25. It is manufactured by DiaDent Group International. The 510(k) number is K210333.
When was DiaPaste approved by the FDA?
DiaPaste received FDA 510(k) clearance on 2021-03-25, under approval number K210333.
What company makes DiaPaste?
DiaPaste is manufactured by DiaDent Group International.
What is the FDA product code for DiaPaste?
The FDA product code for DiaPaste is KIF.
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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.