Acmi Corporation - FDA 510(k) Cleared Devices
Recent clearances: PLASMASEAL OPEN FORCEPS, MODELS 2103PK AND 91701PK, ACMI DUR-HL LASER SYSTEMS, ACMI DUR-DIGITAL URETEROSCOPE AND CHOLEDOCHOSCOPE SYSTEM
16
Total
16
Cleared
0
Denied
FDA 510(k) Regulatory Record - Acmi Corporation Obstetrics & Gynecology ✕
2 devices