FDA 510(k)

Oral-B iO Test Drive Power Brush Trial Program Kit

Номер K: K200881 · 2020-08-27

Дата решения2020-08-27

Код продуктаJEQ

Консультативный комитетDE

РешениеSubstantially Equivalent

Описание устройства

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.

Часто задаваемые вопросы

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.

Связанные клинические исследования

Связанные записи сопоставляются автоматически на основании названий, кодов продукции или иных метаданных. Сопоставление не подтверждает клиническую, научную, корпоративную или регуляторную связь; ознакомьтесь с официальными источниками по ссылкам.

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Другие записи, где The Procter & Gamble Company указан как заявитель

K203567Oral-B Dry Mouth Oral Rinse K201277Oral-B Dry Mouth Oral Rinse

Официальный источник

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