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 Microsystems (Schweiz) AG

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories1
Latest FDA decision2018-09-07
TypeNumberDevice NameCodeDateActions
510(k) K181537 GLOW800IZI2018-09-07 View
510(k) K170239 Leica FL560IZI2017-07-05 View