Advanced Dental Applicance
K-Number: K172991 · 2018-07-10
ApplicantDasoft Partners
Decision Date2018-07-10
Product CodeLRK
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Advanced Dental Applicance is a medical device manufactured by Dasoft Partners. It received FDA 510(k) clearance on 2018-07-10 under approval number K172991. The device is classified under product code LRK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Advanced Dental Applicance?
Advanced Dental Applicance is a medical device that received FDA 510(k) clearance on 2018-07-10. It is manufactured by Dasoft Partners. The 510(k) number is K172991.
When was Advanced Dental Applicance approved by the FDA?
Advanced Dental Applicance received FDA 510(k) clearance on 2018-07-10, under approval number K172991.
What company makes Advanced Dental Applicance?
Advanced Dental Applicance is manufactured by Dasoft Partners.
What is the FDA product code for Advanced Dental Applicance?
The FDA product code for Advanced Dental Applicance is LRK.
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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.