Genzyme Corporation - FDA 510(k) Cleared Devices
Recent clearances: SEPRAMESH, MODEL 5959-1214, SEPRAMESH IP BIORESORBABLE COATING/PERMANENT MESH, SEPRAGEL ENT BIORESORBABLE PACKING/STENT
6
Total
6
Cleared
0
Denied
FDA 510(k) Regulatory Record - Genzyme Corporation Ear, Nose, Throat ✕
1 devices