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FDA 510(k) Applications Submitted by Sienco, Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K002528
08/16/2000
SONOCLOT COAGULATION & PLATELET FUNCTION ANALYZER SYSTEM WITH SIGNATURE VIEWER OPTION
SIENCO, INC.
K032952
09/22/2003
AIACT KIT
SIENCO, INC.
K984141
11/18/1998
GBACT + KIT
SIENCO, INC.
K223635
12/05/2022
Sonoclot Coagulation & Platelet Function Analyzer System with Sonoclot Viewer
Sienco, Inc.
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