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.

Illumina, Inc.

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

Total Devices2
Categories1
Latest FDA decision2026-08-14
TypeNumberDevice NameCodeDateActions
PMA P230011 Next generation sequencing oncology panel, somatic or germline variant detection systemPQP2026-08-14 View
PMA P160038 Next generation sequencing oncology panel, somatic or germline variant detection systemPQP2023-02-17 View

Related Clinical Trials