510(k) K955223
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 13, 1996
- Date Received
- November 14, 1995
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Antigens, Febrile, Slide And Tube, All Groups, Salmonella Spp.
- Device Class
- Class II
- Regulation Number
- 866.3550
- Review Panel
- MI
- Submission Type