Circle Rubber Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Circle Rubber Corp. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Circle Rubber Corp. has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 5 cleared submissions from 1982 to 1989. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Circle Rubber Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Circle Rubber Corp.
5 devices
Cleared
May 16, 1989
THE SAXON SPERMICIDAL CONDOM W/2 YEAR EXPIRATION
Obstetrics & Gynecology
112d
Cleared
Oct 26, 1988
THE SAXON SPERMICIDAL CONDOM
Obstetrics & Gynecology
75d
Cleared
Oct 20, 1987
PROPHYLACTIC (CONDOM)
Obstetrics & Gynecology
103d
Cleared
Sep 21, 1984
WRINKLE CHAPEAU BLACKY
Obstetrics & Gynecology
87d
Cleared
Mar 05, 1982
CONDOM-MULTIPAL STYLES
Obstetrics & Gynecology
109d