510(k) K926173
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 10, 1993
- Date Received
- December 8, 1992
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Kit, Screening, Staphylococcus Aureus
- Device Class
- Class I
- Regulation Number
- 866.2660
- Review Panel
- MI
- Submission Type