510(k) K183151
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 23, 2019
- Date Received
- November 14, 2018
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Method, Nephelometric, Immunoglobulins (G, A, M)
- Device Class
- Class II
- Regulation Number
- 866.5510
- Review Panel
- IM
- Submission Type