W. L. Gore and Associates, Inc. - FDA 510(k) Cleared Devices
Recent clearances: GORE® ENFORM Biomaterial, GORE Tri-Lumen Catheter, GORE Molding and Occlusion Balloon Catheter
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - W. L. Gore and Associates, Inc. General & Plastic Surgery ✕
1 devices