Documento fuente o registro público
FDA 510(k) K192240 — RAPIDPoint 500e Blood Gas System
FDA 510(k) index record K192240. Device: RAPIDPoint 500e Blood Gas System. Applicant as listed: Siemens Healthcare Diagnostics, Inc.. Decision date: 2020-03-27.
Fuente
"device_name": "RAPIDPoint 500e Blood Gas System"
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Automated FDA record verification
2026-10-20
2026-10-20
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FDA 510(k) public index record K192240.
Device name: RAPIDPoint 500e Blood Gas System. Applicant as listed: Siemens Healthcare Diagnostics, Inc..
Decision date: 2020-03-27. Decision wording: Substantially Equivalent.
Product code: CHL. Regulation: 21 CFR 862.1120. Medical specialty: Clinical Chemistry.
This page reproduces regulator index metadata. The applicant field identifies the submitter and is not a manufacturer identity check. Consult the original FDA record for the decision and associated documents; this index does not verify current commercial availability or clinical performance.
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