Burron Medical Products, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CAVAFIX(R) CENTRAL VENOUS CATHETER KIT W/SUTURE, INTESTOPLANT, CAVAFIX, CENTRAL VENOUS CATHETER KIT
41
Total
40
Cleared
0
Denied
FDA 510(k) Regulatory Record - Burron Medical Products, Inc. Cardiovascular ✕
4 devices