510(k) K172868
K172868 is an FDA 510(k) premarket notification submitted by The Binding Site Group , Ltd. for the device "Optilite C-Reactive Protein Reagent,Optilite C-Reactive Protein Calibrator,Optilite C-Reactive Protein Controls". The FDA issued a decision of Substantially Equivalent on February 28, 2018. The device falls under product code DCN (System, Test, C-Reactive Protein), a Class II device regulated under 21 CFR 866.5270. The Binding Site Group , Ltd. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 28, 2018
- Date Received
- September 20, 2017
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Test, C-Reactive Protein
- Device Class
- Class II
- Regulation Number
- 866.5270
- Review Panel
- IM
- Submission Type