FDA 510(k)

Caphosol® 人工唾液 (32 剂量袋装盒)

K号: K234015 · 2024-03-11

决定日期2024-03-11

产品代码LFD

决定实质等同

器械摘要

Caphosol® Artifical Saliva (32 doses sachet box) is the device name listed in this FDA 510(k) record. The listed applicant is Eusa Pharma (Uk) Limited. It received FDA 510(k) clearance on 2024-03-11 under 510(k) number K234015. The device is classified under product code LFD. FDA Decision: Substantially Equivalent.

常见问题

What is the Caphosol® Artifical Saliva (32 doses sachet box)?

Caphosol® Artifical Saliva (32 doses sachet box) is a medical device that received FDA 510(k) clearance on 2024-03-11. The listed applicant is Eusa Pharma (Uk) Limited. The 510(k) number is K234015.

When did Caphosol® Artifical Saliva (32 doses sachet box) receive FDA 510(k) clearance?

Caphosol® Artifical Saliva (32 doses sachet box) received FDA 510(k) clearance on 2024-03-11, under 510(k) number K234015.

Who is the listed applicant for Caphosol® Artifical Saliva (32 doses sachet box)?

The FDA 510(k) record lists Eusa Pharma (Uk) Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Caphosol® Artifical Saliva (32 doses sachet box)?

The FDA product code for Caphosol® Artifical Saliva (32 doses sachet box) is LFD.

列明Eusa Pharma (Uk) Limited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。

K162167Caphosol 人工唾液片

官方来源

在 FDA 数据库中查看 →

数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。