FDA 510(k)

Luvis 椅子 (LC700C)

K号: K233921 · 2024-09-06

决定日期2024-09-06

产品代码KLC

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决定实质等同

器械摘要

Luvis Chair (LC700C) is the device name listed in this FDA 510(k) record. The listed applicant is Dentis Co., Ltd.. It received FDA 510(k) clearance on 2024-09-06 under 510(k) number K233921. The device is classified under product code KLC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Luvis Chair (LC700C)?

Luvis Chair (LC700C) is a medical device that received FDA 510(k) clearance on 2024-09-06. The listed applicant is Dentis Co., Ltd.. The 510(k) number is K233921.

When did Luvis Chair (LC700C) receive FDA 510(k) clearance?

Luvis Chair (LC700C) received FDA 510(k) clearance on 2024-09-06, under 510(k) number K233921.

Who is the listed applicant for Luvis Chair (LC700C)?

The FDA 510(k) record lists Dentis Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Luvis Chair (LC700C)?

The FDA product code for Luvis Chair (LC700C) is KLC.

列明Dentis Co., Ltd.为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

K253493Dentis SQ-SL AXEL 固定装置 K241065ChecQ (AC100)K241063s-Clean 扫描修复基台 K240511Dentis s-Clean SQ-SL 固定装置 K233544MESHEET K230126Dentis s-Clean 标准牙槽基台

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