Intratherapeutics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: INTRASTENT DOUBLESTRUT LD, MODIFICATION TO INTRASTENT, INTRAMAX ITI GUIDE CATHETER
15
Total
7
Cleared
0
Denied
FDA 510(k) Regulatory Record - Intratherapeutics, Inc. Cardiovascular ✕
2 devices