Technicon Instruments Corp. - FDA 510(k) Cleared Devices
157
Total
156
Cleared
0
Denied
Technicon Instruments Corp. has 156 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 156 cleared submissions from 1976 to 1991. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Technicon Instruments Corp. Filter by specialty or product code using the sidebar.
157 devices
Cleared
Nov 27, 1991
TECHNICON AXON(TM) SYSTEM METHODS ANYALYE HDL CHOL
Chemistry
49d
Cleared
Nov 27, 1991
TECHNICON CHEM 1(TM) SYST (GEN2 SYST)
Chemistry
28d
Cleared
Nov 22, 1991
TECHNICON AXON(TM) SYSTEMS, ALT(P 5-P)/AST(P 5-P)
Chemistry
74d
Cleared
Sep 25, 1991
TECHNICON IMMUNO 1 TM SYSTEM ADDITIONAL ANALYTES
Chemistry
104d
Cleared
Jul 01, 1991
CHEM-LINK DATA BASE MANAGER
Chemistry
31d
Cleared
Sep 27, 1990
TECHNICON CHEM I SYSTEM CARBON DIOXIDE METHOD
Chemistry
65d
Cleared
Sep 27, 1990
DRUG OF ABUSE ANALYSIS SYSTEM FREE RADICAL ASSAY
Toxicology
38d
Cleared
Sep 27, 1990
DRUG OF ABUSE ANALYSIS SYSTEM
Toxicology
38d
Cleared
Aug 29, 1990
TECHNICON CHEM I SYSTEM MAGNESIUM METHOD
Chemistry
36d
Cleared
Jul 17, 1990
TECHNICON RA-2000(TM) SYSTEM
Chemistry
113d
Cleared
Jul 05, 1990
TECHNICON IMMUNO I(TM) SYSTEM AND ANALYTES
Chemistry
48d
Cleared
May 14, 1990
CHEM I CLINICAL ANALYZER URINE MAGNESIUM
Chemistry
63d
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