Procter & Gamble Mfg. Co. - FDA 510(k) Cleared Devices

Procter & Gamble Mfg., Co. is a consumer health and personal care manufacturer headquartered in McHenry, US. The company has a long history of developing products across multiple healthcare categories.

The company received 72 FDA 510(k) clearances from 72 total submissions, with no denied submissions on record. Regulatory activity spans from 1976 to 1988, establishing a historical record primarily in Obstetrics & Gynecology and Gastroenterology & Urology device categories. The company is inactive in the FDA 510(k) clearance database, with no submissions recorded in the past several decades.

Historical cleared devices include menstrual pads, pantiliners, incontinence briefs, protective garments, and patient underpads. These products reflect the company's focus on absorbent personal care and continence management devices.

For detailed information on specific device names, product codes, and individual clearance dates, explore the complete regulatory record in the FDA 510(k) database.