Cooper Medical Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cooper Medical Corp. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Cooper Medical Corp. has 5 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 5 cleared submissions from 1982 to 1984.
Browse the FDA 510(k) cleared devices submitted by Cooper Medical Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cooper Medical Corp.
5 devices
Cleared
May 18, 1984
YAG LASER 8000 GASTROINTESTINAL BLEE
Gastroenterology & Urology
126d
Cleared
Apr 18, 1984
ARGON LASER SURGICAL SYSTEM 770
General & Plastic Surgery
202d
Cleared
Apr 17, 1984
COOPER MEDICAL MODEL 770
Neurology
189d
Cleared
Jan 30, 1984
ARGON LASER SYS-MODEL 5000
Ophthalmic
172d
Cleared
Mar 05, 1982
MONITOR CO2 LASER SYSTEM
Obstetrics & Gynecology
31d