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.

Telectronics and Cordis Pacing Systems

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K883265 MODEL 329-701 BIPOLAR ACTIVE-FIXATION LEADDTB1988-10-14 View
510(k) K881904 CHANGE TO CATHODE POWDER SPECIFICATIONDXY1988-07-22 View
510(k) K881711 VICOR MODELS 410B & 410D AND MODIFIED 410A PACEMA.DXY1988-05-26 View
↑