Medical Device Manufacturer · DK , Greve

Hertart - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2013
2
Total
2
Cleared
0
Denied

FDA 510(k) Regulatory Record - Hertart Obstetrics & Gynecology ✕

2 devices
1-2 of 2
Cleared Jul 20, 2015
Micro well group culture dish, 9-well
K150756 · MQK
Obstetrics & Gynecology · 119d
Cleared Jul 03, 2013
CULTURE DISH 40 MM, CULTURE DISH 60 MM, MICRO DROPLET CULTURE DISH, 5 WELL...
K123641 · MQK
Obstetrics & Gynecology · 219d
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