Medical Device Manufacturer · SE , Knivsta

Pharma System AB - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2021
1
Total
1
Cleared
0
Denied

Pharma System AB has 1 FDA 510(k) cleared medical devices. Based in Knivsta, SE.

Last cleared in 2021. Active since 2021. Primary specialty: General Hospital.

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

510(k) submissions have been managed by MEDIcept, Inc. as regulatory consultant.

FDA 510(k) Regulatory Record - Pharma System AB
1 devices
1-1 of 1
Filters
All1 General Hospital 1