510(k) K945642
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 25, 1995
- Date Received
- November 16, 1994
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Fibrin Split Products
- Device Class
- Class II
- Regulation Number
- 864.7320
- Review Panel
- HE
- Submission Type