Promex, Inc. - FDA 510(k) Cleared Devices
Recent clearances: BIOPSY SITE TISSUE MARKER DEVICE, CO-AXIAL INTRODUCER NEEDLE, VACUUM ASSISTED CORE BIOPSY DEVICE
18
Total
18
Cleared
0
Denied
FDA 510(k) Regulatory Record - Promex, Inc. Ophthalmic ✕
1 devices