Documento fuente o registro público
FDA 510(k) K243871 — Philips IntelliSite Pathology Solution 5.1
FDA 510(k) index record K243871. Device: Philips IntelliSite Pathology Solution 5.1. Applicant as listed: Philips Medical Systems Nederland B.V.. Decision date: 2025-03-06.
Fuente
"device_name": "Philips IntelliSite Pathology Solution 5.1"
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2026-10-20
2026-10-25
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FDA 510(k) public index record K243871.
Device name: Philips IntelliSite Pathology Solution 5.1. Applicant as listed: Philips Medical Systems Nederland B.V..
Decision date: 2025-03-06. Decision wording: Substantially Equivalent.
Product code: PSY. Regulation: 21 CFR 864.3700. Medical specialty: Pathology.
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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