510(k) K122304
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- April 15, 2013
- Date Received
- August 1, 2012
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Complement C1 Inhibitor (Inactivator), Antigen, Antiserum, Control
- Device Class
- Class II
- Regulation Number
- 866.5250
- Review Panel
- IM
- Submission Type