Isys Medizintechnik GmbH is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Isys Medizintechnik GmbH - FDA 510(k) Cleared Devices
Recent clearances: Micromate™ Navi+, MICROMATE
3
Total
3
Cleared
0
Denied
Isys Medizintechnik GmbH has 3 FDA 510(k) cleared medical devices. Based in Stamford, US.
Last cleared in 2023. Active since 2014. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Isys Medizintechnik GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Cdi Regulatory Consultants as regulatory consultant.
FDA 510(k) Regulatory Record - Isys Medizintechnik GmbH
3 devices