510(k) K082049
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 5, 2008
- Date Received
- July 18, 2008
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Hepatitis A Test (Antibody And Igm Antibody)
- Device Class
- Class II
- Regulation Number
- 866.3310
- Review Panel
- MI
- Submission Type