Siemens Heatlhcare Diagnostics, Inc. is one of 24174 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Siemens Heatlhcare Diagnostics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DIMENSION MYCOPHENOLIC ACID (MPAT) FLEX REAGENT CARTRIDGE, DIMENSION MYCOPHENOLIC ACID CALIBRATOR (MPAT CAL), DIMENSION VISA HBA1C, MODEL K3105A, ADVIA CENTAUR CALIBRATOR 30, MODELS 10379811/10379810
3
Total
3
Cleared
0
Denied
Siemens Heatlhcare Diagnostics, Inc. has 3 FDA 510(k) cleared medical devices. Based in New York, US.
Historical record: 3 cleared submissions from 2010 to 2011. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Siemens Heatlhcare Diagnostics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Siemens Heatlhcare Diagnostics, Inc.
3 devices