Instrumentation Laboratory CO is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Instrumentation Laboratory CO - FDA 510(k) Cleared Devices
Recent clearances: ACL TOP 970 CL, HemosIL CL Anti-Cardiolipin IgM, HemosIL CL Anti-ß2 Glycoprotein-I IgM, HemosIL Liquid Anti-Xa, GEM Premier ChemSTAT
321
Total
320
Cleared
1
Denied
Instrumentation Laboratory CO has 320 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Last cleared in 2023. Active since 1976.
Browse the FDA 510(k) cleared devices submitted by Instrumentation Laboratory CO Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Instrumentation Laboratory CO
321 devices
Cleared
Sep 29, 2023
ACL TOP 970 CL, HemosIL CL Anti-Cardiolipin IgM, HemosIL CL Anti-ß2...
Hematology
506d
Cleared
Jun 23, 2023
HemosIL Liquid Anti-Xa
Hematology
254d
Cleared
Jan 27, 2023
GEM Premier ChemSTAT
Chemistry
119d
Cleared
Dec 09, 2022
HemosIL von Willebrand Factor Antigen
Hematology
30d
Cleared
Oct 04, 2022
HemosIL Liquid Anti-Xa
Hematology
341d
Cleared
Aug 16, 2022
HemosIL ReadiPlasTin
Hematology
299d
Cleared
Aug 20, 2021
GEM Premier 5000
Chemistry
235d
Not Cleared
Sep 17, 2020
HemosIL Liquid Anti-Xa
Hematology
450d
Cleared
Aug 19, 2020
HemosIL von Willebrand Factor Antigen
Hematology
225d
Cleared
Feb 16, 2019
GEM Premier ChemSTAT
Chemistry
58d
Cleared
Feb 16, 2019
GEM Premier ChemSTAT
Chemistry
58d
Cleared
Feb 16, 2019
GEM Premier ChemSTAT
Chemistry
58d
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