Medikro OY is one of 47 FDA 510(k) medical device manufacturers from Finland in the dataset, ranked by real submission volume.
Medikro OY - FDA 510(k) Cleared Devices
Recent clearances: MEDIKRO SPIROSTAR, M929 Medikro Spirostar USB and M921 Medikro SpiroStar DX, MEDIKRO NANO, MEDIKRO PRIMO AND MEDIKRO PRO
2
Total
2
Cleared
0
Denied
Medikro OY has 2 FDA 510(k) cleared medical devices. Based in Kuopio, FI.
Historical record: 2 cleared submissions from 2014 to 2015. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Medikro OY Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medikro OY
2 devices