510(k) K162977
K162977 is an FDA 510(k) premarket notification submitted by Siemens Healthcare Diagnostics for the device "ADVIA 2120i, ADVIA 2120". The FDA issued a decision of Substantially Equivalent on Aug 11, 2017. The device falls under product code GKZ (Counter, Differential Cell), a Class II device regulated under 21 CFR 864.5220. Siemens Healthcare Diagnostics has 245 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Aug 11, 2017
- Date Received
- Oct 26, 2016
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Counter, Differential Cell
- Device Class
- Class II
- Regulation Number
- 864.5220
- Review Panel
- HE
- Submission Type
- 510(k)