Sienco, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Sienco, Inc. has 5 FDA 510(k) cleared medical devices. Based in Broomfield, US.
Last cleared in 2023. Active since 1995. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by Sienco, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Sienco, Inc.
5 devices
Cleared
Jan 04, 2023
Sonoclot Coagulation & Platelet Function Analyzer System with Sonoclot Viewer
Hematology
30d
Cleared
Dec 12, 2003
AIACT KIT
Hematology
81d
Cleared
Aug 31, 2000
SONOCLOT COAGULATION & PLATELET FUNCTION ANALYZER SYSTEM WITH SIGNATURE...
Hematology
15d
Cleared
May 28, 1999
GBACT + KIT
Hematology
191d
Cleared
Sep 05, 1995
SONOCLOT COAGULATION & PLATELET FUNCTION ANALYZER
Hematology
95d