Vasca, Inc. - FDA 510(k) Cleared Devices
Recent clearances: LIFESITE HEMODIALYSIS ACCESS SYSTEM/CANNULA EXCHANGE, MODEL LHAS14120 & LHCEK0000
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Vasca, Inc. Gastroenterology & Urology ✕
2 devices