Cardio Design Pty. , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: PERITRON PERINEOMETER MODEL 9300V OR 9300A, PERITRON
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Cardio Design Pty. , Ltd. Gastroenterology & Urology ✕
2 devices