Ortho Pharmaceutical Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ortho Pharmaceutical Corp. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Ortho Pharmaceutical Corp. has 9 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 9 cleared submissions from 1979 to 1996.
Browse the FDA 510(k) cleared devices submitted by Ortho Pharmaceutical Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ortho Pharmaceutical Corp.
9 devices
Cleared
Jun 21, 1996
K-Y PERSONAL LUBRICANT
Obstetrics & Gynecology
192d
Cleared
Feb 24, 1994
ADVANCE PREGNANCY TEST MODIFICATION
Chemistry
160d
Cleared
Dec 23, 1991
ADVANCE(R) PREGNANCY TEST
Chemistry
46d
Cleared
Oct 31, 1989
PULSATILE PUMP FOR GONADORELIN ACETATE
General Hospital
180d
Cleared
Apr 06, 1988
MICROSCRAPE
General & Plastic Surgery
20d
Cleared
Mar 17, 1981
FACT* HOME PREGNANCY TEST
Chemistry
14d
Cleared
Apr 29, 1980
NICKERSON'S MED. SELECTIVE CULTURE MEDIU
Microbiology
25d
Cleared
Jan 16, 1980
CONCEPTROL/THIN PROPHYLACTICS
Obstetrics & Gynecology
28d
Cleared
Feb 01, 1979
LUBRICANT, OTRHO PERSONAL
General Hospital
15d