Hach CM130 Chlorine Monitoring System— 510(k) K162471

Name: FDA 510(k) clearance K162471
Creator: U.S. Food and Drug Administration
Published: 2017-03-30

Substantially Equivalent

Hach Company

FDA 510(k) clearance K162471 for Hach CM130 Chlorine Monitoring System, Substantially Equivalent on 2017-03-30. Applicant: Hach Company. Device class: 2.

Clearance details

Applicant: Hach Company
Product code: Code PSX
Device class: Class 2
Regulation: 21 CFR 876.5665
Advisory panel: Gastroenterology, Urology
Date received: 2016-09-06
Decision date: 2017-03-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ames, IA, US

Download summary PDF View on FDA.gov ↗

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