Alcyone Lifesciences, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K172006 | Alivio Ventricular Catheter and Flusher System (Alivio System) | November 9, 2017 |
| K150660 | Alcyone MEMS Cannula (AMC) System | April 16, 2015 |