510(k) K172590
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 2, 2018
- Date Received
- August 29, 2017
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Separator, Automated, Blood Cell And Plasma, Therapeutic
- Device Class
- Class U
- Regulation Number
- Review Panel
- GU
- Submission Type