510(k) K960147
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 12, 1996
- Date Received
- January 11, 1996
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Antisera, All Groups, Salmonella Spp.
- Device Class
- Class II
- Regulation Number
- 866.3550
- Review Panel
- MI
- Submission Type