Medical Device Manufacturer · US , Mchenry , IL

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

72 submissions · 72 cleared · Since 1976

Official Website

72

Total

72

Cleared

0

Denied

FDA 510(k) Regulatory Record - Procter & Gamble Mfg. Co. General Hospital ✕

27 devices

1-12 of 27

Cleared Jul 02, 1986

SINGLE-USE PATIENT UNDERPAD

General Hospital · 12d

Cleared Oct 16, 1985

ATTENDS DISPOS. UNDERPAD

General Hospital · 28d

Cleared Jan 14, 1985

SURGICAL DRAPES

General Hospital · 34d

Cleared Aug 17, 1984

BOUNDARY SINGLE-USE OR GOWN

General Hospital · 21d

Cleared May 01, 1984

BOUNDARY SINGLE-USE GOWNS

General Hospital · 141d

Cleared Jan 25, 1984

SINGLE-USE SURGICAL DRAPES

General Hospital · 78d

Cleared Nov 12, 1980

BOUNDARY SURGICAL DRAPES WITH ADHESIVE

General Hospital · 19d

Cleared Sep 26, 1980

BOUNDARY SINGLE-USE DRAPE

General Hospital · 18d

Cleared Sep 26, 1980

BOUNDARY SINGLE-USE DRAPES

General Hospital · 16d

Cleared Sep 26, 1980

BOUNDARY SINGLE-USE DRAPES

General Hospital · 10d

Cleared Aug 04, 1980

NON-CONDUCTIVE SHOE COVERS

General Hospital · 20d

Cleared Aug 04, 1980

CONDUCTIVE SHOE COVERS

General Hospital · 20d