Medical Device Manufacturer · DE , Vorstetten

Steinhart Medizinsysteme GmbH - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2005
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.

FDA 510(k) Regulatory Record - Steinhart Medizinsysteme GmbH
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