Medical Device Manufacturer · US , Newark , DE

Jostra Medizintechnik AG - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2000

Total

Cleared

Denied

Jostra Medizintechnik AG has 2 FDA 510(k) cleared medical devices. Based in Newark, US.

Historical record: 2 cleared submissions from 2000 to 2000. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Jostra Medizintechnik AG Filter by specialty or product code using the sidebar.

Jostra Medizintechnik AG is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Jostra Medizintechnik AG

2 devices

1-2 of 2