FDA 510(k)

els超低收缩率®复合材料 & els超低收缩率®流动

K号: K240823 · 2024-06-27

决定日期2024-06-27

产品代码EBF

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决定实质等同

器械摘要

els extra low shrinkage® composite & els extra low shrinkage® flow is the device name listed in this FDA 510(k) record. The listed applicant is Saremco Dental AG. It received FDA 510(k) clearance on 2024-06-27 under 510(k) number K240823. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the els extra low shrinkage® composite & els extra low shrinkage® flow?

els extra low shrinkage® composite & els extra low shrinkage® flow is a medical device that received FDA 510(k) clearance on 2024-06-27. The listed applicant is Saremco Dental AG. The 510(k) number is K240823.

When did els extra low shrinkage® composite & els extra low shrinkage® flow receive FDA 510(k) clearance?

els extra low shrinkage® composite & els extra low shrinkage® flow received FDA 510(k) clearance on 2024-06-27, under 510(k) number K240823.

Who is the listed applicant for els extra low shrinkage® composite & els extra low shrinkage® flow?

The FDA 510(k) record lists Saremco Dental AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for els extra low shrinkage® composite & els extra low shrinkage® flow?

The FDA product code for els extra low shrinkage® composite & els extra low shrinkage® flow is EBF.

列明Saremco Dental AG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。

K252151els unibond K232050赛美科打印桥德克 K213343Saremco Print CROWNTEC

官方来源

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