Medical Device Manufacturer · US , Mason , OH

Procter & Gamble

2 submissions · 2 cleared · Since 2008

Total

Cleared

Denied

Procter & Gamble — FDA 510(k) Submissions

Procter & Gamble has submitted 2 FDA 510(k) premarket notifications since 2008, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Toothbrush, Manual, Pessary, Vaginal . Use the specialty filter in the sidebar to narrow results.

2 devices

1–2 of 2

Always/Tampax bladder supports

K151413 · HHW Pessary, Vaginal · Obstetrics & Gynecology

Dec 2015 205d

ORAL-B SUB-BRAND MANUAL TOOTHBRUSH

K073224 · EFW Toothbrush, Manual · Dental

Feb 2008 83d

Data Source

FDA 510(k) public files . 174,402 total devices indexed.

Procter & Gamble

Procter & Gamble — FDA 510(k) Submissions

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