Diality, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Moda-flx Hemodialysis System™ Cartridge (102121-001 ), Moda-flx Hemodialysis System and Cartridge
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Diality, Inc. Gastroenterology & Urology ✕
2 devices