Medifactia AB - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Medifactia AB has 2 FDA 510(k) cleared medical devices. Based in Gothenburg, SE.
Last cleared in 2023. Active since 2019. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Medifactia AB Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Msquared Associates, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Medifactia AB
2 devices