510(k) K000755
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 9, 2000
- Date Received
- March 8, 2000
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Anti-Sm Antibody, Antigen And Control
- Device Class
- Class II
- Regulation Number
- 866.5100
- Review Panel
- IM
- Submission Type