Hach Company
FDA Regulatory Profile
Hach Company appears in FDA public data with 0 recalls, 4 510(k) clearances, 3 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 30, 2017.
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 |