Clearance Summary
ADVIA 2120 WITH AUTOSLIDE SYSTEM, AND ADVIA 2120I received FDA 510(k) clearance under submission number K102644, sponsored by Siemens Healthcare Diagnostics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 2011-11-23.
- Submission: K102644
- Applicant / Sponsor: Siemens Healthcare Diagnostics
- Clearance pathway: Traditional
- Review panel: Hematology
- Device class: Class II
- Regulation citation: 21 CFR 864.5220
- Decision date: 2011-11-23
Classification & Regulation
This clearance is catalogued under FDA product code GKZ and 21 CFR 864.5220, within the Hematology review panel as a Class II device.