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.

Embol-X, Inc.

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

Total Devices4
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K022071 EMBOL-X AORTIC FILTERS,ETRA-SMALL,SMALL,MEDIUM,LARGE,EXTRA LARGE,MODELS CF26000.CF29000,CF32000,CF35000,CF4000DTM2003-02-14 View
510(k) K020693 AORTIC CANNULA, METAL J-TIP (24FR) MODEL #CF00100; AORTIC CANNULA, PLASTIC J-TIP (24FR) MODEL #CF00101DWF2002-09-05 View
510(k) K002973 EMBOL-X INTRODUCER, MODEL CF00200DYB2001-04-26 View
510(k) K980631 EMBOL-X AORTIC OCCLUSION AND CARDIOPLEGIA CANNULADXC1999-02-02 View
↑