Siemens Helathcare Diagnostics, Inc. is one of 5157 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Siemens Helathcare Diagnostics, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Siemens Helathcare Diagnostics, Inc. has 2 FDA 510(k) cleared medical devices. Based in West Sacramento, US.
Historical record: 2 cleared submissions from 2013 to 2013. Primary specialty: Immunology.
Browse the FDA 510(k) cleared devices submitted by Siemens Helathcare Diagnostics, Inc. Filter by specialty or product code using the sidebar.
Siemens Helathcare Diagnostics, Inc. — FDA 510(k) Products and Clearance History
2 devices
Cleared
Nov 08, 2013
MICROSCAN DRIED GRAM-POSTIVE MIC/COMBO PANELS
Microbiology
189d
Cleared
Sep 20, 2013
IMMULITE 2000 ANTI-TG AB CALIBRATION VERIFICATION MATERIAL, IMMULITE 2000...
Immunology
50d