FDA 510(k)

Oral-B 干口漱口水

K号: K201277 · 2020-09-02

决定日期2020-09-02

产品代码LFD

决定实质等同

器械摘要

Oral-B Dry Mouth Oral Rinse is the device name listed in this FDA 510(k) record. The listed applicant is The Procter & Gamble Company. It received FDA 510(k) clearance on 2020-09-02 under 510(k) number K201277. The device is classified under product code LFD. FDA Decision: Substantially Equivalent.

常见问题

What is the Oral-B Dry Mouth Oral Rinse?

Oral-B Dry Mouth Oral Rinse is a medical device that received FDA 510(k) clearance on 2020-09-02. The listed applicant is The Procter & Gamble Company. The 510(k) number is K201277.

When did Oral-B Dry Mouth Oral Rinse receive FDA 510(k) clearance?

Oral-B Dry Mouth Oral Rinse received FDA 510(k) clearance on 2020-09-02, under 510(k) number K201277.

Who is the listed applicant for Oral-B Dry Mouth Oral Rinse?

The FDA 510(k) record lists The Procter & Gamble Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Oral-B Dry Mouth Oral Rinse?

The FDA product code for Oral-B Dry Mouth Oral Rinse is LFD.

列明The Procter & Gamble Company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。

K203567Oral-B 干口漱口水 K200881Oral-B iO 测试驾驶功率刷试用程序套装

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。