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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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