Medical Device Manufacturer · IT , Pisa

Thyssenkrupp Ceteco Srl - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2009

Total

Cleared

Denied

Thyssenkrupp Ceteco Srl has 2 FDA 510(k) cleared medical devices. Based in Pisa, IT.

Historical record: 2 cleared submissions from 2009 to 2010. Primary specialty: Physical Medicine.

Browse the FDA 510(k) cleared devices submitted by Thyssenkrupp Ceteco Srl Filter by specialty or product code using the sidebar.

Thyssenkrupp Ceteco Srl is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Thyssenkrupp Ceteco Srl

2 devices

1-2 of 2