Steinhart Medizinsysteme GmbH is one of 516 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Steinhart Medizinsysteme GmbH - FDA 510(k) Cleared Devices
Recent clearances: HIPAX MEDICAL IMAGING SOFTWARE
1
Total
1
Cleared
0
Denied
Steinhart Medizinsysteme GmbH has 1 FDA 510(k) cleared medical devices. Based in Vorstetten, DE.
Historical record: 1 cleared submissions from 2005 to 2005. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Steinhart Medizinsysteme GmbH 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 - Steinhart Medizinsysteme GmbH
1 devices