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.

Chf Solutions, Inc.

FDA 510(k) & PMA Approved Devices — 13 products

Total Devices13
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K192756 Aquadex FlexFlow System 2.0KDI2020-02-24 View
510(k) K071854 AQUADEX FLEXFLOW SYSTEMKDI2007-09-07 View
510(k) K070512 MODIFICATION TO AQUADEX FLEXFLOW SYSTEMKDI2007-04-27 View
510(k) K062922 MODIFICATION TO AQUADEX FLEXFLOW SYSTEMKDI2006-12-13 View
510(k) K060008 AQUADEX FLEXFLOW SYSTEMKDI2006-02-02 View
510(k) K050609 AQUADEX SYSTEMKDI2005-11-09 View
510(k) K041791 5.2F DUAL LUMEN EXTENDED LENGTH CATHETER (DELC)NQJ2004-09-10 View
510(k) K040489 AQUADEX SYSTEM 100, MODEL A1100KDI2004-04-27 View
510(k) K031689 DUAL LUMEN EXTENDED LENGTH CATHETER (DELC)NQJ2003-12-23 View
510(k) K023874 SYSTEM 100 ULTRAFILTRATION CATHETERKDI2003-11-20 View
510(k) K024124 SYSTEM 100-UF 500 CIRCUIT WITH IN-LINE NEEDLELESS ACCESS PORTKDI2003-03-14 View
510(k) K023224 INFUSION CATHETER EXTENSION SETKDI2002-10-25 View
510(k) K013733 SYSTEM 100; S-100 ULTRAFILTRATION CONSOLE; BDT 500 ULTRAFILTRATION SETKDI2002-06-03 View
↑