Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Leica Biosystems Imaging, Inc.

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4
Categories2
Latest FDA decision2026-08-07
TypeNumberDevice NameCodeDateActions
510(k) K253554 Aperio GT 450 DX; Aperio GT 180 DXPSY2026-08-07 View
510(k) K253561 Aperio iQC DX SoftwareQKQ2026-08-07 View
510(k) K232202 Aperio GT 450 DXPSY2024-04-16 View
510(k) K190332 Aperio AT2 DX SystemPSY2019-05-20 View