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.

Diality, Inc.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K243607 Moda-flx Hemodialysis System™ Cartridge (102121-001 )FJK2024-12-20 View
510(k) K233798 Moda-flx Hemodialysis System and CartridgeKDI2024-08-02 View
↑