510(k) K935554
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 30, 1995
- Date Received
- November 17, 1993
- Clearance Type
- Traditional
- 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