FDA 510(k)

Apapro脱敏剂

K号: K220419 · 2022-02-16

决定日期2022-02-16

产品代码LBH

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决定实质等同

器械摘要

Apapro Desensitizer is the device name listed in this FDA 510(k) record. The listed applicant is Sangi Co., Ltd.. It received FDA 510(k) clearance on 2022-02-16 under 510(k) number K220419. The device is classified under product code LBH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Apapro Desensitizer?

Apapro Desensitizer is a medical device that received FDA 510(k) clearance on 2022-02-16. The listed applicant is Sangi Co., Ltd.. The 510(k) number is K220419.

When did Apapro Desensitizer receive FDA 510(k) clearance?

Apapro Desensitizer received FDA 510(k) clearance on 2022-02-16, under 510(k) number K220419.

Who is the listed applicant for Apapro Desensitizer?

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

What is the FDA product code for Apapro Desensitizer?

The FDA product code for Apapro Desensitizer is LBH.

列明Sangi 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。

K260830APAPRO 家用脱敏剂（再矿化抗敏感牙膏）

官方来源

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