MESHEET
K-Number: K233544 · 2024-02-22
ApplicantDentis Co., Ltd.
Decision Date2024-02-22
Product CodeNXC
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
MESHEET is a medical device manufactured by Dentis Co., Ltd.. It received FDA 510(k) clearance on 2024-02-22 under approval number K233544. The device is classified under product code NXC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the MESHEET?
MESHEET is a medical device that received FDA 510(k) clearance on 2024-02-22. It is manufactured by Dentis Co., Ltd.. The 510(k) number is K233544.
When was MESHEET approved by the FDA?
MESHEET received FDA 510(k) clearance on 2024-02-22, under approval number K233544.
What company makes MESHEET?
MESHEET is manufactured by Dentis Co., Ltd..
What is the FDA product code for MESHEET?
The FDA product code for MESHEET is NXC.
Other Devices by Dentis Co., Ltd.
Related Devices (Code: NXC)
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.