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Procter & Gamble Mfg. Co.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
72
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K873036ATTENDS INCONTINENT BRIEFJanuary 19, 1988
K873457SCENTED OR SCENTED DEODORIZED MENSTRUAL PADSJanuary 19, 1988
K864673UNSCENTED MENSTRUAL PADJanuary 21, 1987
K861863MODIFIED PROTECTIVE GARMENTAugust 11, 1986
K862348SINGLE-USE PATIENT UNDERPADJuly 2, 1986
K860598MODIFIED PROTECTIVE GARMENT FOR INCONTINENTSMarch 5, 1986
K853880ATTENDS DISPOS. UNDERPADOctober 16, 1985
K853000SCENTED ALWAYS PANTILINERSSeptember 6, 1985
K852985UNSCENTED ALWAYS PANTILINERSAugust 29, 1985
K850940ALWAYS SUPER MAXIPAD-UNSCENTEDMay 14, 1985
K850939ALWAYS SUPER MAXIPAD-SCENTEDMay 14, 1985
K850956ALWAYS MAXIPADS - SCENTEDMay 14, 1985
K850955ALWAYS MAXIPADS - UNSCENTEDMay 14, 1985
K850611ATTENDS INCONTINENT UNDERGARMENTFebruary 26, 1985
K844601UNSCENTED MENSTRUAL PADJanuary 16, 1985
K844602SCENTED MENSTRUAL PADJanuary 16, 1985
K844802SURGICAL DRAPESJanuary 14, 1985
K844757TUBING HOLDERDecember 17, 1984
K842958BOUNDARY SINGLE-USE OR GOWNAugust 17, 1984
K842763UNSCENTED MENSTRUAL PADAugust 10, 1984