FDA 510(k) Applications Submitted by JOSEPH P DEPAOLO

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
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.


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