Prodeon Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Urocross Expander System (Model Numbers ES2018 and ES3025), Prodeon Urethral Sheath System
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Prodeon Medical, Inc. Gastroenterology & Urology ✕
3 devices