The Procter & Gamble Co. is one of 20726 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
The Procter & Gamble Co. - FDA 510(k) Cleared Devices
Recent clearances: TAMPAX C PLASTIC TAMPONS, UNSCENTED, VICKS POWERSHOT DRY THROAT & MOUTH RELIEF
2
Total
2
Cleared
0
Denied
The Procter & Gamble Co. has 2 FDA 510(k) cleared medical devices. Based in Mason, US.
Historical record: 2 cleared submissions from 2009 to 2011. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by The Procter & Gamble Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - The Procter & Gamble Co.
2 devices