Browne Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Browne Corp. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Browne Corp. has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 7 cleared submissions from 1979 to 1979. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Browne Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Browne Corp.
7 devices
Cleared
Dec 06, 1979
BROWNE MODEL UD-4
Gastroenterology & Urology
50d
Cleared
Dec 06, 1979
BROWNE MODEL UD-4D
Gastroenterology & Urology
50d
Cleared
Dec 06, 1979
BROWNE MODEL UD-4E
Gastroenterology & Urology
50d
Cleared
Dec 06, 1979
BROWNE MODEL GD-5
Gastroenterology & Urology
50d
Cleared
Dec 06, 1979
BROWNE MODEL UA-6
Gastroenterology & Urology
50d
Cleared
Jun 01, 1979
BROWNE MODEL UD-4DE
Gastroenterology & Urology
84d
Cleared
Jun 01, 1979
BROWNE MODEL CF-1 AND CF-1G
Gastroenterology & Urology
45d