Documento fuente o registro público
FDA 510(k) K260964 — NanoZoomer S540MD Slide Scanner System
FDA 510(k) index record K260964. Device: NanoZoomer S540MD Slide Scanner System. Applicant as listed: Hamamatsu Photonics K.K.. Decision date: 2026-07-22.
Fuente
"device_name": "NanoZoomer S540MD Slide Scanner System"
Esta entrada describe lo que cubre el documento; el propio documento es la autoridad. Incluirlo no implica estar de acuerdo con sus conclusiones.
Review and references
Automated FDA record verification
2026-10-20
2026-10-22
professional use
FDA 510(k) public index record K260964.
Device name: NanoZoomer S540MD Slide Scanner System. Applicant as listed: Hamamatsu Photonics K.K..
Decision date: 2026-07-22. 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.
Interested in these solutions?
Submit a sourcing request with the assays, volumes, and timeline of your own project.