Procter & Gamble Mfg. Co. - FDA 510(k) Cleared Devices
Recent clearances: ATTENDS INCONTINENT BRIEF, SCENTED OR SCENTED DEODORIZED MENSTRUAL PADS, UNSCENTED MENSTRUAL PAD
72
Total
72
Cleared
0
Denied
FDA 510(k) Regulatory Record - Procter & Gamble Mfg. Co. Pathology ✕
1 devices