Siemens is one of 26109 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Siemens - FDA 510(k) Cleared Devices
Recent clearances: MICROSCAN DRIED GRAM-POSITIVE MIC/COMBO PANELS NEW ANTIMICROBIAL TEST - INDUCIBLE CLINDAMYCIN
1
Total
1
Cleared
0
Denied
Siemens, is a global technology company with a manufacturing facility in West Sacramento, US. The company develops industrial automation, digitalization, and electrification solutions serving customers worldwide.
Siemens has received #1# FDA 510(k) clearance from #1# total submission in the Microbiology device category. The company's cleared device, MICROSCAN DRIED GRAM-POSITIVE MIC/COMBO PANELS NEW ANTIMICROBIAL TEST - INDUCIBLE CLINDAMYCIN, was approved in 2008. This represents a historical regulatory record; Siemens has not pursued additional FDA 510(k) clearances since that time.
Explore the complete device name, product code, and clearance date in the full regulatory database record.
FDA 510(k) Regulatory Record - Siemens
1 devices