510(k) K811828
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 12, 1981
- Date Received
- June 29, 1981
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Test, Sickle Cell
- Device Class
- Class II
- Regulation Number
- 864.7825
- Review Panel
- HE
- Submission Type