Medical Device Manufacturer · US , Mt. Laurel , NJ

Sopro - Acteon Group - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2014

4

Total

4

Cleared

0

Denied

FDA 510(k) Regulatory Record - Sopro - Acteon Group Obstetrics & Gynecology ✕

1 devices

1-1 of 1

Cleared Jun 17, 2016

S698 Symbioz flow

Obstetrics & Gynecology · 207d