Advanced Uroscience, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Advanced Uroscience, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Advanced Uroscience, Inc. has 5 FDA 510(k) cleared medical devices. Based in St, Paul, US.
Historical record: 5 cleared submissions from 1998 to 2001. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Advanced Uroscience, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Advanced Uroscience, Inc.
5 devices
Cleared
May 03, 2001
TISSUE MARKER
General & Plastic Surgery
322d
Cleared
Nov 16, 2000
ADVANCED UROSCIENCE INNERSHEATH
Gastroenterology & Urology
90d
Cleared
Jul 31, 2000
ADVANCED UROSCIENCE INJECTION NEEDLE
Gastroenterology & Urology
34d
Cleared
Nov 05, 1999
MODIFICATION TO BRENNEN BIOSYNTHETIC SURGICAL MESH MATRIX
Gastroenterology & Urology
23d
Cleared
Oct 26, 1998
ADVANCED UROSCIENCE INJECTION NEEDLE
Gastroenterology & Urology
70d