Transformair, LLC is one of 18968 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Transformair, LLC - FDA 510(k) Cleared Devices
Recent clearances: Transformair Indoor Air Purifier
1
Total
1
Cleared
0
Denied
Transformair, LLC has 1 FDA 510(k) cleared medical devices. Based in Tampa, US.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Transformair, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Transformair, LLC
1 devices