510(k) K913668
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 20, 1991
- Date Received
- August 19, 1991
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Ceruloplasmin, Antigen, Antiserum, Control
- Device Class
- Class II
- Regulation Number
- 866.5210
- Review Panel
- IM
- Submission Type