FDA 510(k) Applications Submitted by TRUDY D ESTRIDGE

FDA 510(k) Number Submission Date Device Name Applicant
K070610 03/05/2007 SKATER BILIARY CATHETER ANGIOTECH
DEN090007 04/17/2009 BIO-SEAL LUNG BIOPSY TRACT SYSTEM ANGIOTECH
K073672 12/27/2007 SKATER BILIARY CATHETER ANGIOTECH
K080680 03/10/2008 QUILL SELF-RETAINING SYSTEM (SRS) COMPRISED OF PDO (POLYDIOXANONE SURGICAL SPECIALTIES CORP.
K080985 04/07/2008 QUILL SELF-RETAINING SYSTEM (SRS) COMPRISED OF POLYDIOXANONE (PDO) SURGICAL SPECIALTIES CORP.
K101832 07/01/2010 BIOPINCE ULTRA FULL CORE BIOPSY INSTRUMENT MEDICAL DEVICE TECHNOLOGIES, INC.
K073520 12/14/2007 ANGIOTECH CVC ANGIOTECH PHARMACEUTICALS, INC.


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