FDA 510(k)

PF 保持；Cad Cam 保持块

K号: K233171 · 2023-11-27

决定日期2023-11-27

产品代码EBI

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决定实质等同

器械摘要

PF Keep; Cad Cam Keep Block is the device name listed in this FDA 510(k) record. The listed applicant is Clemde SA DE CV. It received FDA 510(k) clearance on 2023-11-27 under 510(k) number K233171. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the PF Keep; Cad Cam Keep Block?

PF Keep; Cad Cam Keep Block is a medical device that received FDA 510(k) clearance on 2023-11-27. The listed applicant is Clemde SA DE CV. The 510(k) number is K233171.

When did PF Keep; Cad Cam Keep Block receive FDA 510(k) clearance?

PF Keep; Cad Cam Keep Block received FDA 510(k) clearance on 2023-11-27, under 510(k) number K233171.

Who is the listed applicant for PF Keep; Cad Cam Keep Block?

The FDA 510(k) record lists Clemde SA DE CV as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PF Keep; Cad Cam Keep Block?

The FDA product code for PF Keep; Cad Cam Keep Block is EBI.

列明Clemde SA DE CV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。

K242897Partial Flex

官方来源

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