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.

Thomas Medical Products, Inc.

FDA 510(k) & PMA Approved Devices — 23 products

Total Devices23
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K122431 HEARTSPAN STEERABLE INTRODUCER KITDYB2013-01-29 View
510(k) K120158 CORONARY SINUS GUIDE AND LATERAL VEIN INTRODUCER KITSDYB2012-08-14 View
510(k) K101015 GUIDE CATHETERS AND ACCESSORIESDQY2010-09-23 View
510(k) K083269 CROSSOVERDYB2009-02-03 View
510(k) K081341 REINFORCED CATHETER INTRODUCER SYSTEM (RCIS)DYB2008-05-14 View
510(k) K072745 Y-GLIDEDTL2008-01-04 View
510(k) K043438 LARGE BORE SPLITTABLE INTRODUCER KITDYB2005-02-15 View
510(k) K040713 MODIFICATION TO BRAIDED GUIDING INTRODUCER SYSTEMDYB2004-06-01 View
510(k) K011727 TRANSSEPTAL NEEDLE/TROCARDRC2002-05-02 View
510(k) K020090 MODIFICATION TO TRANSSEPTAL INTRODUCER SETDYB2002-02-11 View
510(k) K013202 MODIFICATION TO BRAIDED GUIDING INTRODUCERDYB2001-10-23 View
510(k) K004025 SPLITTABLE SHEATH INTRODUCER KITDYB2001-07-19 View
510(k) K004026 BRAIDED GUIDING INTRODUCERDYB2001-07-09 View
510(k) K003731 SAFESHEATH MSP INTRODUCER SHEATH KIT WITH INTEGRAL HEMOSTASIS VALVEDYB2001-04-10 View
510(k) K961780 HEMODIALYSIS INTRODUCER SETDYB1996-12-24 View
510(k) K961466 PERCUTANEOUS INTRODUCER SETDYB1996-09-12 View
510(k) K934901 TEAR-AWAY SHEATH INTRODUCER SET WITH INTEGRAL HEMOSTASIS VALVEDYB1994-01-21 View
510(k) K931587 MULTI-PORT Y INTRODUCER SETDYB1993-10-06 View
510(k) K932619 TRANSSEPTAL INTRODUCER SETDQY1993-08-24 View
510(k) K924456 LONG LENGTH PERCUTANEOUS INTRODUCER SETDYB1993-03-22 View
↑