Credo is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
1
Total
1
Cleared
0
Denied
Credo has 1 FDA 510(k) cleared medical devices. Based in Wonju-Si, KR.
Last cleared in 2021. Active since 2021. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Credo Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by KMC, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Credo
1 devices