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.

Neumodx Molecular, Inc.

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

Total Devices2
Categories2
Latest FDA decision2023-12-22
TypeNumberDevice NameCodeDateActions
510(k) K230267 NeuMoDx CT/NG Assay 2.0QEP2023-12-22 View
510(k) K173725 NeuMoDx GBS AssayNJR2018-06-26 View
↑