Source document or public record
FDA 510(k) K221900 — Stat Profile Prime Plus Analyzer System
FDA 510(k) index record K221900. Device: Stat Profile Prime Plus Analyzer System. Applicant as listed: Nova Biomedical Corporation. Decision date: 2023-09-29.
Source
"device_name": "Stat Profile Prime Plus Analyzer System"
This entry describes what the document covers; the document itself is the authority. Listing it is not agreement with its conclusions.
Review and references
Automated FDA record verification
2026-10-20
2026-10-20
professional use
FDA 510(k) public index record K221900.
Device name: Stat Profile Prime Plus Analyzer System. Applicant as listed: Nova Biomedical Corporation.
Decision date: 2023-09-29. 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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