FDA 510(k)

Oral-B iO 测试驾驶功率刷试用程序套装

K号: K200881 · 2020-08-27

决定日期2020-08-27

产品代码JEQ

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决定实质等同

器械摘要

Oral-B iO Test Drive Power Brush Trial Program Kit 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 2020-08-27 under 510(k) number K200881. The device is classified under product code JEQ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Oral-B iO Test Drive Power Brush Trial Program Kit?

Oral-B iO Test Drive Power Brush Trial Program Kit is a medical device that received FDA 510(k) clearance on 2020-08-27. The listed applicant is The Procter & Gamble Company. The 510(k) number is K200881.

When did Oral-B iO Test Drive Power Brush Trial Program Kit receive FDA 510(k) clearance?

Oral-B iO Test Drive Power Brush Trial Program Kit received FDA 510(k) clearance on 2020-08-27, under 510(k) number K200881.

Who is the listed applicant for Oral-B iO Test Drive Power Brush Trial Program Kit?

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 iO Test Drive Power Brush Trial Program Kit?

The FDA product code for Oral-B iO Test Drive Power Brush Trial Program Kit is JEQ.

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 K201277Oral-B 干口漱口水

官方来源

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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。

器械摘要

常见问题

相关临床试验

列明The Procter & Gamble Company为申报人的其他记录

官方来源