510(k) K102286
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 20, 2011
- Date Received
- August 12, 2010
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Antisera, Latex Agglutination, Cryptococcus Neoformans
- Device Class
- Class II
- Regulation Number
- 866.3165
- Review Panel
- MI
- Submission Type