Clearance Summary
RAPIDPoint 500e Blood Gas System received FDA 510(k) clearance under submission number K192240, sponsored by Siemens Healthcare Diagnostics, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2020-03-27.
- Submission: K192240
- Applicant / Sponsor: Siemens Healthcare Diagnostics, Inc.
- Clearance pathway: Special
- Review panel: Clinical Chemistry
- Device class: Class II
- Regulation citation: 21 CFR 862.1120
- Decision date: 2020-03-27
Classification & Regulation
This clearance is catalogued under FDA product code CHL and 21 CFR 862.1120, within the Clinical Chemistry review panel as a Class II device.