FHC, Inc. - FDA 510(k) Cleared Devices
Recent clearances: STarFix Designer Software C0265, VFS1 Bipolar Electrosurgical Generator, microTargeting Guideline 4000 5.0 System
12
Total
12
Cleared
0
Denied
FDA 510(k) Regulatory Record - FHC, Inc. General & Plastic Surgery ✕
1 devices