510(k) K990046
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 17, 1999
- Date Received
- January 7, 1999
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Plasma, Coagulation Factor Deficient
- Device Class
- Class II
- Regulation Number
- 864.7290
- Review Panel
- HE
- Submission Type