Objective 

To evaluate the efficacy of the 7000 series and the Plasma BAR in reducing Influenza A (H1N1) virus. 

Methodology 

The 0.2 m³ acrylic test chamber was put into biological safety cabinet. The D5 device and fan were then placed in the test chamber. The virus suspensions were sprayed into the chamber using a compressor-type nebulizer NE-C16 (OMRON) into the test chamber for 5 minutes at an air flow ratio of approximately 0.2 mL/min. 

Summary of Results 

The device reduced 86.6% of Influenza A virus after one hour.