Cuptimize, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Cuptimize, Inc. has 1 FDA 510(k) cleared medical devices. Based in Belleair Bluffs, US.
Last cleared in 2021. Active since 2021. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Cuptimize, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mcra, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Cuptimize, Inc.
1 devices