Inter Medical Medizintechnik GmbH is one of 474 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Inter Medical Medizintechnik GmbH - FDA 510(k) Cleared Devices
Recent clearances: UniCam Evo Software, MULTICAM 3000 ECO, CX 250 C PLUS WITH GAMMAXP SOFTWARE, MODEL 0121 0000
3
Total
3
Cleared
0
Denied
Inter Medical Medizintechnik GmbH has 3 FDA 510(k) cleared medical devices. Based in Luebbecke, DE.
Last cleared in 2023. Active since 2005. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Inter Medical Medizintechnik GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Inter Medical Medizintechnik GmbH
3 devices