Analyticon Biotechnologies AG is one of 23863 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Analyticon Biotechnologies AG - FDA 510(k) Cleared Devices
Recent clearances: COMBI SCAN 500 URINE TEST STRIP ANALYZER, MODEL A93005, COMBI SCAN100, COMBI-SCREEN, MODELS 10SL AND 11SL
3
Total
3
Cleared
0
Denied
Analyticon Biotechnologies AG has 3 FDA 510(k) cleared medical devices. Based in Deer Field, US.
Historical record: 3 cleared submissions from 2003 to 2007. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Analyticon Biotechnologies AG Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Analyticon Biotechnologies AG
3 devices