Source document or public record
FDA 510(k) K232018 — Citrated: K, KH, RTH, FFH
FDA 510(k) index record K232018. Device: Citrated: K, KH, RTH, FFH. Applicant as listed: Haemonetics Corporation. Decision date: 2024-03-29.
Source
"device_name": "Citrated: K, KH, RTH, FFH"
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
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FDA 510(k) public index record K232018.
Device name: Citrated: K, KH, RTH, FFH. Applicant as listed: Haemonetics Corporation.
Decision date: 2024-03-29. Decision wording: Substantially Equivalent.
Product code: JPA. Regulation: 21 CFR 864.5425. Medical specialty: Hematology.
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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