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Aerocrine AB

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K150233NIOX VERO Airway Inflammation MonitorFebruary 26, 2015
K133898NIOX VERO AIRWAY INFLAMMATION MONITORNovember 6, 2014
K123683NIOX PANEL FOR USE WITH THE NIOX MINO AIRWAY INFLAMMATION MONITORDecember 27, 2012
K101034NIOX MINO MODEL 09-1000September 2, 2010
K072816NIOX MINOMarch 3, 2008
DEN030001NIOX ARTICLE NO: 02-1000April 30, 2003