The Procter & Gamble Co.

The Procter & Gamble Co. holds 2 FDA 510(k) medical device clearances, first cleared 2009, most recent 2011.

Top product codes for The Procter & Gamble Co.

HEB — Obstetrics/Gynecology1 device
LFD — Unknown1 device

Recent clearances by The Procter & Gamble Co.

K110669 — TAMPAX C PLASTIC TAMPONS, UNSCENTEDCode HEB·2011-06-02
K091419 — VICKS POWERSHOT DRY THROAT & MOUTH RELIEFCode LFD·2009-08-28

Data sourced from openFDA. This site is unofficial and independent of the FDA.