Medical Device Manufacturer · KR , Wonju-Si

Credo - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2021
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
1-1 of 1
Filters
All1 Cardiovascular 1