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Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Procter & Gamble Mfg. Co. — Predicate Candidate Screening

72 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

25 daysmedian FDA review time
68 days90th percentile
72clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K873457SCENTED OR SCENTED DEODORIZED MENSTRUAL PADSProcter & Gamble Mfg. Co.1988-01-191440
K873036ATTENDS INCONTINENT BRIEFProcter & Gamble Mfg. Co.1988-01-191680
K864673UNSCENTED MENSTRUAL PADProcter & Gamble Mfg. Co.1987-01-21500
K861863MODIFIED PROTECTIVE GARMENTProcter & Gamble Mfg. Co.1986-08-11880
K862348SINGLE-USE PATIENT UNDERPADProcter & Gamble Mfg. Co.1986-07-02120
K860598MODIFIED PROTECTIVE GARMENT FOR INCONTINENTSProcter & Gamble Mfg. Co.1986-03-05140
K853880ATTENDS DISPOS. UNDERPADProcter & Gamble Mfg. Co.1985-10-16280
K853000SCENTED ALWAYS PANTILINERSProcter & Gamble Mfg. Co.1985-09-06530
K852985UNSCENTED ALWAYS PANTILINERSProcter & Gamble Mfg. Co.1985-08-29450
K850939ALWAYS SUPER MAXIPAD-SCENTEDProcter & Gamble Mfg. Co.1985-05-14680
K850940ALWAYS SUPER MAXIPAD-UNSCENTEDProcter & Gamble Mfg. Co.1985-05-14680
K850956ALWAYS MAXIPADS - SCENTEDProcter & Gamble Mfg. Co.1985-05-14670
K850955ALWAYS MAXIPADS - UNSCENTEDProcter & Gamble Mfg. Co.1985-05-14670
K850611ATTENDS INCONTINENT UNDERGARMENTProcter & Gamble Mfg. Co.1985-02-26110
K844602SCENTED MENSTRUAL PADProcter & Gamble Mfg. Co.1985-01-16500
K844601UNSCENTED MENSTRUAL PADProcter & Gamble Mfg. Co.1985-01-16500
K844802SURGICAL DRAPESProcter & Gamble Mfg. Co.1985-01-14340
K844757TUBING HOLDERProcter & Gamble Mfg. Co.1984-12-17100
K842958BOUNDARY SINGLE-USE OR GOWNProcter & Gamble Mfg. Co.1984-08-17210
K842764SCENTED MENSTRUAL PADProcter & Gamble Mfg. Co.1984-08-10250
K842763UNSCENTED MENSTRUAL PADProcter & Gamble Mfg. Co.1984-08-10250
K834332BOUNDARY SINGLE-USE GOWNSProcter & Gamble Mfg. Co.1984-05-011410
K841255BOUNDARY SINGLE-USE GOWNSProcter & Gamble Mfg. Co.1984-04-25300
K834339BOUNDARY REINFORCED SINGLE-USE GOWNSProcter & Gamble Mfg. Co.1984-03-05840
K834296ADULT INCONTINENCE BRIEFProcter & Gamble Mfg. Co.1984-02-04580
K834295ADULT INCONTINENCE PADProcter & Gamble Mfg. Co.1984-02-04580
K833877SINGLE-USE SURGICAL DRAPESProcter & Gamble Mfg. Co.1984-01-25780
K834131SCENTED MENSTRUAL PADProcter & Gamble Mfg. Co.1983-12-29280
K834144UNSCENTED MENSTRUAL PADProcter & Gamble Mfg. Co.1983-12-29280
K831357BOUNDARY HEADWEARProcter & Gamble Mfg. Co.1983-06-02370
K830144PANTY-LINERS SCENTEDProcter & Gamble Mfg. Co.1983-01-2140
K830145PANTY-LINERS UNSCENTEDProcter & Gamble Mfg. Co.1983-01-2140
K823478SCENTED MENSTRUAL PADSProcter & Gamble Mfg. Co.1983-01-18560
K823477UNSCENTED MENSTRUAL PADSProcter & Gamble Mfg. Co.1983-01-18560
K812651X-RAY DETECTABLE LAP SPONGESProcter & Gamble Mfg. Co.1981-10-20330
K812403SCENTED MENSTRUAL PADSProcter & Gamble Mfg. Co.1981-09-09200
K812402UNSCENTED MENSTRUAL PADSProcter & Gamble Mfg. Co.1981-09-09200
K811868SCENTED MENSTRUAL PADSProcter & Gamble Mfg. Co.1981-07-16150
K811869UNSCENTED MENSTRUAL PADSProcter & Gamble Mfg. Co.1981-07-16150
K802652BOUNDARY SURGICAL DRAPES WITH ADHESIVEProcter & Gamble Mfg. Co.1980-11-12190
K802148BOUNDARY SINGLE-USE DRAPEProcter & Gamble Mfg. Co.1980-09-26180
K802247BOUNDARY SINGLE-USE DRAPESProcter & Gamble Mfg. Co.1980-09-26100
K802192BOUNDARY SINGLE-USE DRAPESProcter & Gamble Mfg. Co.1980-09-26160
K801617CONDUCTIVE SHOE COVERSProcter & Gamble Mfg. Co.1980-08-04200
K801616NON-CONDUCTIVE SHOE COVERSProcter & Gamble Mfg. Co.1980-08-04200
K801132BOUNDARY EXTREMITY DRAPEProcter & Gamble Mfg. Co.1980-05-2080
K800272RELY DEODERANT TAMPONProcter & Gamble Mfg. Co.1980-02-26190
K792631STERILIZATION PROCESS/DBL. GRIP CORD CLPProcter & Gamble Mfg. Co.1980-01-28400
K792627STERILIZATION PROCESS/MATERNITY PADProcter & Gamble Mfg. Co.1980-01-28400
K792632STERILIZATION PROCESS/BULB SYRINGEProcter & Gamble Mfg. Co.1980-01-16280

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda