Medical Device Manufacturer · DE , Bonn

Sicat GmbH & Co. KG - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 2006

Recent clearances: SICAT Implant V2.0, SICAT Endo

Total

Cleared

Denied

Sicat GmbH & Co. KG has 9 FDA 510(k) cleared medical devices. Based in Bonn, DE.

Historical record: 9 cleared submissions from 2006 to 2019. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Sicat GmbH & Co. KG Filter by specialty or product code using the sidebar.

Sicat GmbH & Co. KG is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Sicat GmbH & Co. KG

9 devices

1-9 of 9

GALILEOS IMPLANT, VERSION 1.7

GALILEOS IMPLANT, V 1.0

K061472 · LLZ

Radiology · 10d

Sicat GmbH & Co. KG - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Sicat GmbH & Co. KG

Filters