510(k) K952139
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 18, 1995
- Date Received
- May 8, 1995
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Antigens (Febrile), Agglutination, Brucella Spp.
- Device Class
- Class II
- Regulation Number
- 866.3085
- Review Panel
- MI
- Submission Type