Medical Device Manufacturer · SE , Kristianstad

Cresco TI Systems AB - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2001

Total

Cleared

Denied

Cresco TI Systems AB has 2 FDA 510(k) cleared medical devices. Based in Kristianstad, SE.

Historical record: 2 cleared submissions from 2001 to 2004. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Cresco TI Systems AB Filter by specialty or product code using the sidebar.

Cresco TI Systems AB is one of 59 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Cresco TI Systems AB

2 devices

1-2 of 2