FDA 510(k) Applications Submitted by JOSEPH P DE PAOLO

FDA 510(k) Number Submission Date Device Name Applicant
K121070 04/09/2012 C-QUR RPM MESH ATRIUM MEDICAL CORP.
K121301 05/01/2012 XPRESSWAY RX CATHETER (6F LD-VERISON) KANEKA PHARMA AMERICA LLC
K070192 01/22/2007 ATRIUM PROLITE ULTRA S MESH ATRIUM MEDICAL CORP.
K050311 02/08/2005 ATRIUM MEDICAL CORPORATION C-QUR MESH ATRIUM MEDICAL CORP.
K060396 02/15/2006 IVENA VASCULAR PATCH ATRIUM MEDICAL CORP.
K080688 03/11/2008 C-QUR LITE MESH V-PATCH ATRIUM MEDICAL CORP.
K080691 03/11/2008 C-QUR EDGE MESH V-PATCH ATRIUM MEDICAL CORP.
K090909 04/01/2009 C-QUR V -PATCH MESH ATRIUM MEDICAL CORP.
K041269 05/12/2004 ATRIUM MEDICAL CORPORATION ICAST COVERED STENT ATRIUM MEDICAL CORP.
K002093 07/11/2000 ATRIUM LITE MESH ATRIUM MEDICAL CORP.
K992776 08/18/1999 UNI-GRAFT K DV PATCH ATRIUM MEDICAL CORP.
K082748 09/19/2008 ATRIUM PROLITE S MESH ATRIUM MEDICAL CORP.
K043140 11/15/2004 EXPRESS AND OASIS CHEST DRAIN ATRIUM MEDICAL CORP.
K043582 12/28/2004 OCEAN CHEST DRAIN ATRIUM MEDICAL CORP.
K061680 06/15/2006 ATRIUM MEDICAL CORPORATION CLEARWAY RX CATHETER ATRIUM MEDICAL CORP.
K984496 12/17/1998 ATRIUM MEDICAL CORPORATION EXPRESS CHEST DRAIN ATRIUM MEDICAL CORP.
K060129 01/18/2006 IGS VAGINAL SPECULUM INNOVATIVE GYNECOLOGICAL SOLUTIONS LLC
K050814 03/31/2005 ATRIUM ICAST COVERED STENT ATRIUM MEDICAL CORP.
K013577 10/29/2001 ULTRAMAX WOVEN VELOUR VASCULAR GRAFT ATRIUM MEDICAL CORP.


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