510(k) K173376
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 14, 2018
- Date Received
- October 30, 2017
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Antigens, Nontreponemal, All
- Device Class
- Class II
- Regulation Number
- 866.3820
- Review Panel
- MI
- Submission Type