510(k) K002215
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 28, 2000
- Date Received
- July 24, 2000
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Test System, Antineutrophil Cytoplasmic Antibodies (Anca)
- Device Class
- Class II
- Regulation Number
- 866.5660
- Review Panel
- IM
- Submission Type