Luvis Chair (LC700C)
K-Number: K233921 · 2024-09-06
ApplicantDentis Co., Ltd.
Decision Date2024-09-06
Product CodeKLC
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Luvis Chair (LC700C) is a medical device manufactured by Dentis Co., Ltd.. It received FDA 510(k) clearance on 2024-09-06 under approval number K233921. The device is classified under product code KLC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Luvis Chair (LC700C)?
Luvis Chair (LC700C) is a medical device that received FDA 510(k) clearance on 2024-09-06. It is manufactured by Dentis Co., Ltd.. The 510(k) number is K233921.
When was Luvis Chair (LC700C) approved by the FDA?
Luvis Chair (LC700C) received FDA 510(k) clearance on 2024-09-06, under approval number K233921.
What company makes Luvis Chair (LC700C)?
Luvis Chair (LC700C) is manufactured by Dentis Co., Ltd..
What is the FDA product code for Luvis Chair (LC700C)?
The FDA product code for Luvis Chair (LC700C) is KLC.
Other Devices by Dentis Co., Ltd.
Related Devices (Code: KLC)
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.