Adam Spence Corp. - FDA 510(k) Cleared Devices
Recent clearances: EZ-INTRO PERCUTANEOUS CATHETER SHEATH, EZ-INTRO VESSEL DILATOR, MAXI-TORQUE PLUS ANGIOGRAPHIC CATHETER
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Adam Spence Corp. Cardiovascular ✕
3 devices