Q Urological Corporation - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Q Urological Corporation has 3 FDA 510(k) cleared medical devices. Based in Natick, US.
Historical record: 3 cleared submissions from 2010 to 2017. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Q Urological Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Q Urological Corporation
3 devices
Cleared
Oct 04, 2017
pAguaMedicina PERSISTENT Structural Hydrogel Ureteral Stent
Gastroenterology & Urology
65d
Cleared
Dec 22, 2016
pAguaMedicina PERSISTENT Structural Hydrogel Ureteral Stent
Gastroenterology & Urology
50d
Cleared
Jan 20, 2010
PAGUAMEDICINA STRUCTURAL HYDROGEL PEDIATRIC URETERAL STENT, MODEL NP330-XXX
Gastroenterology & Urology
483d