FDA 510(k)

Oral-B iO Test Drive Power Brush Trial Program Kit

K-Number: K200881 · 2020-08-27

Decision Date2020-08-27

Product CodeJEQ

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

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.

Frequently Asked Questions

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.

Other records listing The Procter & Gamble Company as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.