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Airsonett, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K130702
AIRSONETT AIR-4
July 23, 2013
K081062
AIRSONNETT AIRSHOWER AIR 3
November 7, 2008