Cooper Medical Devices Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cooper Medical Devices Corp. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Cooper Medical Devices Corp. has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 7 cleared submissions from 1979 to 1981. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Cooper Medical Devices Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cooper Medical Devices Corp.
7 devices
Cleared
Feb 05, 1981
SEBESTYEN IRRIGATING CONTACT LENS
Ophthalmic
78d
Cleared
Feb 05, 1981
LANDERS CONTACT LENS
Ophthalmic
76d
Cleared
Sep 16, 1980
CHARLES PNEUMATIC INTRAOCULAR SCISSORS
Ophthalmic
43d
Cleared
Jul 21, 1980
MAY ILLUMINATED/INFUSION PIC
Ophthalmic
35d
Cleared
Jun 17, 1980
THE PROTECTORS
General & Plastic Surgery
14d
Cleared
May 14, 1980
VABRA ASPIRATOR
Obstetrics & Gynecology
30d
Cleared
Oct 30, 1979
OCUTOME MODEL 8000
Ophthalmic
35d