Bluezone Products, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Bluezone Products, Inc. has 1 FDA 510(k) cleared medical devices. Based in Woburn, US.
Last cleared in 2022. Active since 2022. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Bluezone Products, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by O'Connell Regulatory Consultant, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Bluezone Products, Inc.
1 devices