Prodeon Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Urocross Expander System (Model Numbers ES2018 and ES3025), Prodeon Urethral Sheath System
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Prodeon Medical, Inc. Gastroenterology & Urology ✕
2 devices