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