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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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