Rosch AG Medizintechnic is one of 516 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Rosch AG Medizintechnic - FDA 510(k) Cleared Devices
Recent clearances: INJEX NEEDLE-FREE INJECTION SYSTEM
1
Total
1
Cleared
0
Denied
Rosch AG Medizintechnic has 1 FDA 510(k) cleared medical devices. Based in Berlin, DE.
Historical record: 1 cleared submissions from 2002 to 2002. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Rosch AG Medizintechnic 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 - Rosch AG Medizintechnic
1 devices