510(k) K010523
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 15, 2001
- Date Received
- February 22, 2001
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Antisera, All Groups, Streptococcus Spp.
- Device Class
- Class I
- Regulation Number
- 866.3740
- Review Panel
- MI
- Submission Type