Brasamerica Medical Equipment, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ICEL ULTRASONIC NEBULIZER MODELS PU 12000 AIR AND PU 12300 AIR
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Brasamerica Medical Equipment, Inc. Anesthesiology ✕
2 devices