Source document or public record
FDA 510(k) K231017 — Panther Fusion AdV/hMPV/RV Assay
FDA 510(k) index record K231017. Device: Panther Fusion AdV/hMPV/RV Assay. Applicant as listed: Hologic, Inc.. Decision date: 2023-05-05.
Source
"device_name": "Panther Fusion AdV/hMPV/RV Assay"
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 K231017.
Device name: Panther Fusion AdV/hMPV/RV Assay. Applicant as listed: Hologic, Inc..
Decision date: 2023-05-05. Decision wording: Substantially Equivalent.
Product code: OCC. Regulation: 21 CFR 866.3980. Medical specialty: Microbiology.
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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