Medical Device Manufacturer · SE , Vaxjo

Arcoma AB - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2008
2
Total
2
Cleared
0
Denied

Arcoma AB has 2 FDA 510(k) cleared medical devices. Based in Vaxjo, SE.

Historical record: 2 cleared submissions from 2008 to 2014. Primary specialty: Radiology.

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

FDA 510(k) Regulatory Record - Arcoma AB
2 devices
1-2 of 2
Cleared Jun 03, 2014
0180 INTUITION, 0072 PRECISION
K140683 · KPR
Radiology · 77d
Cleared Jan 10, 2008
INTUITION, MODEL 0170
K073632 · KPR
Radiology · 15d
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