Source document or public record
FDA 510(k) K201778 — i-STAT TBI Plasma cartridge with the i-STAT Alinity System
FDA 510(k) index record K201778. Device: i-STAT TBI Plasma cartridge with the i-STAT Alinity System. Applicant as listed: Abbott Laboratories. Decision date: 2021-01-08.
Source
"device_name": "i-STAT TBI Plasma cartridge with the i-STAT Alinity System"
This entry describes what the document covers; the document itself is the authority. Listing it is not agreement with its conclusions.
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2026-10-20
2026-10-20
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FDA 510(k) public index record K201778.
Device name: i-STAT TBI Plasma cartridge with the i-STAT Alinity System. Applicant as listed: Abbott Laboratories.
Decision date: 2021-01-08. Decision wording: Substantially Equivalent.
Product code: QAT. Regulation: 21 CFR 866.5830. Medical specialty: Immunology.
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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