Medical Device Manufacturer · KR , Seoul

Papricalab - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2023
1
Total
1
Cleared
0
Denied

Papricalab has 1 FDA 510(k) cleared medical devices. Based in Seoul, KR.

Last cleared in 2023. Active since 2023. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Papricalab Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Gms Consulting as regulatory consultant.

FDA 510(k) Regulatory Record - Papricalab
1 devices
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