510(k) K052143
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 4, 2005
- Date Received
- August 8, 2005
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Antibodies, Gliadin
- Device Class
- Class II
- Regulation Number
- 866.5750
- Review Panel
- IM
- Submission Type