510(k) K023131
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 21, 2003
- Date Received
- September 9, 2002
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Lambda, Antigen, Antiserum, Control
- Device Class
- Class II
- Regulation Number
- 866.5550
- Review Panel
- IM
- Submission Type