Medical Device Manufacturer · SE , Stockholm, Sweden

Eureka AB - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1988

Total

Cleared

Denied

Eureka AB has 1 FDA 510(k) cleared medical devices. Based in Stockholm, Sweden, SE.

Historical record: 1 cleared submissions from 1988 to 1988. Primary specialty: Cardiovascular.

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

Eureka AB is one of 59 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Eureka AB

1 devices

1-1 of 1