Weyerhaeuser Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Weyerhaeuser Co. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Weyerhaeuser Co. has 10 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 10 cleared submissions from 1981 to 1989. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Weyerhaeuser Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Weyerhaeuser Co.
10 devices
Cleared
Jan 30, 1989
DRIPRIDE PROVIDE SLIM
Gastroenterology & Urology
138d
Cleared
Jan 30, 1989
DRIPRIDE ULTRA INCONTINENT PAD
Gastroenterology & Urology
138d
Cleared
Jun 03, 1988
DRIPRIDE DISPOSABLE UNDERPAD
General Hospital
31d
Cleared
Mar 16, 1988
DRIPRIDE PROVIDE ULTRA
Gastroenterology & Urology
293d
Cleared
May 15, 1987
DRIPRIDE DISPOSABLE UNDERPADS
General Hospital
11d
Cleared
Nov 19, 1985
ADULT ABSORBENT INCONTINENT BRIEF
Gastroenterology & Urology
18d
Cleared
Mar 05, 1984
ABSORBENT INCONTINENT PADS & BRIEFS
Gastroenterology & Urology
83d
Cleared
Aug 12, 1983
MAXI SHIELDS
Obstetrics & Gynecology
87d
Cleared
Feb 08, 1983
UNSCENTED PANTY SHIELDS
Obstetrics & Gynecology
15d
Cleared
Oct 19, 1981
UNSCENTED MENSTRUAL PADS
Obstetrics & Gynecology
40d