Primus Corp. is one of 13039 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Primus Corp. - FDA 510(k) Cleared Devices
Recent clearances: PRIMUS LIQUID CALIBRATOR FOR GHB/A1C LEVEL 1 AND LEVEL 2, PRIMUS LIQUID CONTROL FOR GHB/ALC LEVEL I AND LEVEL II, PRIMUS VARIANT SYSTEM PVS99
11
Total
11
Cleared
0
Denied
Primus Corp. has 11 FDA 510(k) cleared hematology devices. Based in Kansas City, US.
Historical record: 11 cleared submissions from 1994 to 2007.
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) Regulatory Record - Primus Corp.
11 devices
Cleared
Nov 26, 2007
PRIMUS A1CARE ASSAY
Chemistry
446d
Cleared
May 14, 2002
NYCOCARD CRP
Chemistry
181d
Cleared
Jan 07, 2002
NYCOCARD CRP CONTROL
Immunology
27d
Cleared
Dec 21, 1999
PRIMUS LIQUID CALIBRATOR FOR GHB/A1C LEVEL 1 AND LEVEL 2
Hematology
22d
Cleared
Nov 12, 1999
PRIMUS LIQUID CONTROL FOR GHB/ALC LEVEL I AND LEVEL II
Hematology
74d
Cleared
Mar 01, 1996
PRIMUS VARIANT SYSTEM PVS99
Hematology
106d
Cleared
Sep 14, 1994
PRIMUS RAPID GEL 100 GLYCATED HEMOGLOBIN ASSAY
Hematology
142d
Cleared
May 09, 1994
GLYCATED PROTEIN CALIBRATORS
Hematology
125d
Cleared
Apr 26, 1994
GLYCATED PROTEIN CONTROLS
Hematology
105d
Cleared
Mar 22, 1994
GLYCATED HEMOGLOBIN CALIBRATORS
Hematology
83d
Cleared
Mar 15, 1994
GLYCATED HEMOGLOBIN CONTROLS
Hematology
63d