510(k) K855013
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 26, 1986
- Date Received
- December 16, 1985
- 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