Medical Device Manufacturer · KR , Daejon, Korea

Blue Egg CO - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2010
1
Total
1
Cleared
0
Denied

Blue Egg CO has 1 FDA 510(k) cleared medical devices. Based in Daejon, Korea, KR.

Historical record: 1 cleared submissions from 2010 to 2010. Primary specialty: Obstetrics & Gynecology.

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

FDA 510(k) Regulatory Record - Blue Egg CO

1 devices
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