Medical Device Manufacturer · DE , Bonn

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

9 submissions · 9 cleared · Since 2006

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.

FDA 510(k) cleared devices by 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) cleared devices by Sicat GmbH & Co. KG

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