FDA 510(k) Applications Submitted by Amarilys Machado

FDA 510(k) Number Submission Date Device Name Applicant
K010511 02/21/2001 MODIFICATION TO: AGILITY STEERABLE GUIDEWIRES CORDIS NEUROVASCULAR, INC.
K080967 04/04/2008 TRUFILL DCS ORBIT DETACHABLE COIL AND TRUFILL DCS SYRINGE OR TRUFILL DCS SYRINGE II, ALSO KNOWN AS THE TRUFILL DCS ORBIT CORDIS NEUROVASCULAR, INC.
K071962 07/16/2007 VASCULAR OCCLUSION SYSTEM (TRUFILL PUSHABLE COILS AND TRUPUSH COIL PUSHER) CORDIS NEUROVASCULAR, INC.
K132281 07/23/2013 ReVive PV (Peripheral Vasculature) Thrombectomy Device Codman & Shurtleff, Inc.
K082324 08/14/2008 TRUFILL DCS SYRINGE CORDIS NEUROVASCULAR, INC.
K032553 08/19/2003 TRUFILL DCS ORBIT DETACHABLE COIL AND TRUFILL DCS SYRINGE, ALSO KNOWN AS TRUFILL DCS ORBIT DETACHABLE COIL SYSTEM CORDIS NEUROVASCULAR, INC.
K063254 10/27/2006 THE TRUFILL DCS DETACHABLE COIL SYSTEM; THE TRUFILL DCS ORBIT DETACHABLE COIL SYSTEM CORDIS NEUROVASCULAR, INC.
K053197 11/16/2005 TRUFILL DCS ORBIT DETACHABLE COIL SYSTEM LINE EXTENSION CORDIS NEUROVASCULAR, INC.
K003925 12/20/2000 PROWLER INFUSION CATHETERS WITH PRE-SHAPED TIPS CORDIS NEUROVASCULAR, INC.
K093973 12/24/2009 TRUFILL DCS ORBIT DETACHABLE COIL SYSTEM Codman & Shurtleff, Inc.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact