Hach CM130 Chlorine Monitoring System
FDA 510(k) clearance K162471 · decided 2017-03-30
Clearance details
- K-number
- K162471
- Device name
- Hach CM130 Chlorine Monitoring System
- Applicant
- Hach Company
- Decision
- Substantially Equivalent
- Date received
- 2016-09-06
- Decision date
- 2017-03-30
- Days to decision
- 205 days
- Clearance type
- Traditional
- Product code
- PSX
- Device class
- 2
- Regulation number
- 876.5665
- Medical specialty
- Gastroenterology, Urology
- Advisory committee
- Gastroenterology, Urology
- Location
- Ames, IA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.