FDA 510(k) Applications Submitted by HACH COMPANY

FDA 510(k) Number Submission Date Device Name Applicant
K070419 02/13/2007 OPACIDEN OPA REAGENT STRIPS HACH COMPANY
K040660 03/12/2004 STERICHEK GLUTARALDEHYDE REAGENT STRIPS HACH COMPANY
K042322 08/26/2004 STERICHEK BLOOD LEAK REAGENT STRIPS HACH COMPANY
K162471 09/06/2016 Hach CM130 Chlorine Monitoring System HACH COMPANY


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