Pixcell Medical Technologies
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K240636 | HemoScreen Hematology Analyzer | May 2, 2024 |
| K222148 | HemoScreen Hematology Analyzer | August 16, 2023 |
| K180020 | HemoScreen Hematology Analyzer | October 29, 2018 |