Airistar Technologies, LLC is one of 24358 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Airistar Technologies, LLC - FDA 510(k) Cleared Devices
Recent clearances: AIRISTAR AIR PURIFICATION SYSTEM, MODEL 500 & 1000
1
Total
1
Cleared
0
Denied
Airistar Technologies, LLC has 1 FDA 510(k) cleared medical devices. Based in Deer Field, US.
Historical record: 1 cleared submissions from 2008 to 2008. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Airistar Technologies, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Airistar Technologies, LLC
1 devices