R&D Systems, Inc. - FDA 510(k) Cleared Devices
79
Total
79
Cleared
0
Denied
R&D Systems, Inc. has 79 FDA 510(k) cleared hematology devices. Based in Mchenry, US.
Historical record: 79 cleared submissions from 1978 to 2016.
Browse the complete list of FDA 510(k) cleared hematology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by R&D Systems, Inc.
79 devices
Cleared
Sep 01, 2016
BC-5D Hematology Control
Hematology
183d
Cleared
Jul 24, 2013
R&D 5D RETIC HEMATOLOGY CONTROL
Hematology
107d
Cleared
Apr 28, 2011
R&D SYSTEMS BODY FLUID-I HEMATOLOGY CONTROL
Hematology
325d
Cleared
Jan 29, 2010
R & D SYSTEMS XERET HEMATOLOGY CONTROL
Hematology
21d
Cleared
Oct 28, 2009
R&D SYSTEMS TETIC-I PLUS HEMOTOLOGY CONTROL
Hematology
168d
Cleared
Dec 27, 2007
HCT EXTENDED HEMATOLOGY CONTROL, MODEL HCT004
Hematology
44d
Cleared
Nov 26, 2007
CSF AUTOMATED CONTROL, MODELS CSF001, CSF003
Hematology
53d
Cleared
Nov 20, 2007
HC WBC HEMATOLOGY CONTROL, MODEL: WBC00S
Hematology
97d
Cleared
Aug 20, 2007
CBC-5D PLUS RETICS HEMATOLOGY CONTROL, MODELS: 5DR03, 5DR04
Hematology
20d
Cleared
Mar 29, 2007
R&D SICKLE QC CONTROL
Hematology
52d
Cleared
Jul 10, 2006
R&D CBC-3D + CRP HEMATOLOGY CONTROL
Hematology
39d
Cleared
Jun 02, 2006
R&D LH-NRBC HEMATOLOGY CONTROL
Hematology
22d
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