Quantimetrix Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Quantimetrix Corp. - FDA 510(k) Cleared Devices
38
Total
38
Cleared
0
Denied
Quantimetrix Corp. has 38 FDA 510(k) cleared chemistry devices. Based in Mchenry, US.
Historical record: 38 cleared submissions from 1983 to 2015.
Browse the complete list of FDA 510(k) cleared chemistry devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Quantimetrix Corp.
38 devices
Cleared
Apr 10, 2015
AUTION CHECK PLUS
Chemistry
239d
Cleared
May 10, 2012
COMPLETE D 25-OH VITAMIN D CONTROL
Chemistry
195d
Cleared
May 12, 2011
DROPPER A1C DIABETES CONTROL
Chemistry
140d
Cleared
Oct 30, 2006
QUANTIMETRIX NICOSURE COTININE URINE CONTROL
Toxicology
32d
Cleared
Oct 03, 2006
MODIFICATION TO QUANTIMETRIX CARDIASURE CARDIAC MARKER
Chemistry
19d
Cleared
Mar 21, 2006
MODIFICATION TO QUANTIMETRIX URINE DRUGS OF ABUSE CONTROL
Toxicology
32d
Cleared
Oct 30, 2003
GLYCOHEMOSURE HBA1C CONTROL
Chemistry
52d
Cleared
Apr 03, 2003
PRECISET DAT AMPHETAMINE
Toxicology
20d
Cleared
Jun 13, 2002
PRECISET DAT PLUS
Toxicology
42d
Cleared
Mar 08, 2002
MODIFICATION TO LIPOPRINT SYSTEM, LDL SUBFRACTIONS
Chemistry
122d
Cleared
Jul 25, 2001
LIPOPRINT SYSTEM, LDL SUBFRACTIONS
Chemistry
170d
Cleared
Mar 23, 2001
SYNOVIALSCOPICS, SYNOVIAL FLUID CONTROL
Hematology
23d
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