Source document or public record
FDA 510(k) K261364 — Atellica CH Acetaminophen 2 (ACTM)
FDA 510(k) index record K261364. Device: Atellica CH Acetaminophen 2 (ACTM). Applicant as listed: Siemens Healthcare Diagnostics, Inc.. Decision date: 2026-07-24.
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"device_name": "Atellica CH Acetaminophen 2 (ACTM)"
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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Automated FDA record verification
2026-10-20
2026-10-20
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FDA 510(k) public index record K261364.
Device name: Atellica CH Acetaminophen 2 (ACTM). Applicant as listed: Siemens Healthcare Diagnostics, Inc..
Decision date: 2026-07-24. Decision wording: Substantially Equivalent.
Product code: LDP. Regulation: 21 CFR 862.3030. Medical specialty: Clinical Toxicology.
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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