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.

Cordis Corp., A Johnson & Johnson Co.

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K131225 ADROIT GUIDING CATHETERDQY2013-05-29 View
510(k) K091077 OPTEASE VENA CAVA FILTER AND RETRIEVAL CATHETERDTK2010-02-04 View
510(k) K083814 OUTBACK LTD RE-ENTRY CATHETER, MODEL: OTB42120PDU2009-01-13 View
510(k) K062531 ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE AND ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIRENTE2006-09-22 View
↑