Cuattro, LLC is one of 19064 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cuattro, LLC - FDA 510(k) Cleared Devices
Recent clearances: CuattroDR, CUATTRO UNOMD
2
Total
2
Cleared
0
Denied
Cuattro, LLC has 2 FDA 510(k) cleared medical devices. Based in Hoptacong, US.
Historical record: 2 cleared submissions from 2010 to 2016. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Cuattro, 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 - Cuattro, LLC
2 devices