Chesebrough-Pond'S U.S.A. Co. - FDA 510(k) Cleared Devices
33
Total
30
Cleared
0
Denied
Chesebrough-Pond'S U.S.A. Co. has 30 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 30 cleared submissions from 1976 to 1987.
Browse the FDA 510(k) cleared devices submitted by Chesebrough-Pond'S U.S.A. Co. Filter by specialty or product code using the sidebar.
33 devices
Cleared
Jan 28, 1987
RESPIRADYNE II(TM)
Anesthesiology
117d
Cleared
Nov 14, 1986
CHESEBROUGH POND'S HYDROCOLLOID DRESSING
General & Plastic Surgery
115d
Cleared
Jul 05, 1985
CHESEBROUGH-POND'S SEQUENTIAL WOUND DRESSING
General & Plastic Surgery
88d
Cleared
Jul 05, 1985
BLISTERFILM TRANSPARENT DRESSING
General & Plastic Surgery
88d
Cleared
Jun 12, 1985
CHESEBROUGH-PONDS KANGAROO PUMP SET W/EASY-CAP CLO
Gastroenterology & Urology
57d
Cleared
Feb 14, 1985
KANGAROO NASOGASTRIC FEEDING TUBE
Gastroenterology & Urology
157d
Cleared
Jan 15, 1985
CONTINENT STOMA SYSTEM & ACCESSORIES
Ear, Nose, Throat
78d
Cleared
Jan 15, 1985
CHESEBROUGH-POND'S URI-DRAIN MALE URINARY POUCH
Gastroenterology & Urology
20d
Cleared
Jan 02, 1985
FEMALE URINARY INCONTINENCE SYS
Gastroenterology & Urology
146d
Cleared
Jan 02, 1985
KANGAROO ACCESS II ENTERAL FEEDING CONTAINER
Gastroenterology & Urology
23d
Cleared
Nov 08, 1984
ISOLATE ADHESIVE BANDAGE FOR MOIST WOUND
General & Plastic Surgery
91d
Cleared
Nov 08, 1984
ISOLATE ADHESIVE BANDAGE FOR DRY WOUND
General & Plastic Surgery
91d