Microaire Surgical Instruments, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MICROAIRE 1000E SYSTEM, LIGHT DUTY PNEUMATIC INSTRUMENT MODEL NUMBER PAD-100, HEAVY DUTY PNEUMATIC INSTRUMENT MODEL PAD-200, LIGHT DUTY ELECTRI, MICROAIRE POWER ASPIRATION DEVICE PAD SYSTEM
4
Total
4
Cleared
0
Denied
FDA 510(k) Regulatory Record - Microaire Surgical Instruments, Inc. General & Plastic Surgery ✕
2 devices