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Hach Company
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
3
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K162471
Hach CM130 Chlorine Monitoring System
March 30, 2017
K070419
OPACIDEN OPA REAGENT STRIPS
August 31, 2007
K042322
STERICHEK BLOOD LEAK REAGENT STRIPS
December 7, 2004
K040660
STERICHEK GLUTARALDEHYDE REAGENT STRIPS
November 15, 2004