The Urology Group is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
The Urology Group - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
The Urology Group has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1980 to 1984. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by The Urology Group Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - The Urology Group
6 devices
Cleared
Jan 03, 1984
COVERUPS
General & Plastic Surgery
223d
Cleared
Dec 12, 1983
SURGICAL TUBE HOLDER
General & Plastic Surgery
216d
Cleared
Jun 26, 1981
SUCTION WOUND DRAINAGE DEVICE
Gastroenterology & Urology
99d
Cleared
Apr 17, 1981
SURGICAL TUBE HOLDER
General & Plastic Surgery
25d
Cleared
Mar 31, 1981
UROLOGIC TUBE HOLDER
Gastroenterology & Urology
8d
Cleared
Aug 12, 1980
COVER-ALL MALE INCONTINENCE DEVICE
Gastroenterology & Urology
28d