Medical Device Manufacturer · KR , Suwon-Si

Weero Co. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2022

Recent clearances: Apollo Duet (Model : APD-4000)

1
Total
1
Cleared
0
Denied

FDA 510(k) Regulatory Record - Weero Co. General & Plastic Surgery

1 devices
1-1 of 1
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