Iris International, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K093861 | IQ 20 SERIES ANALYZER, IQ 200 SERIES SYSTEM, NAD IQ LAMINA CRADLE | February 5, 2010 |
| K060280 | ICHEM 100 URINE CHEMISTRY ANALYZER | June 13, 2006 |
| K050235 | IQ 200 URINE ANALYZER BODY FLUIDS MODULE | March 23, 2005 |