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FDA 510(k) Applications Submitted by Fernando Di Caprio
FDA 510(k) Number
Submission Date
Device Name
Applicant
K200317
02/07/2020
Support Catheter
QXMedical, LLC
K160561
02/29/2016
Boosting Catheter
QXMEDICAL, LLC
K091624
06/03/2009
STENT GRAFT BALLOON CATHETER
VIA BIOMEDICAL, INC.
K123311
10/25/2012
QXMEDICAL ACCESS & SUPPORT CATHETER
QXMEDICAL, LLC
K183679
12/28/2018
Occlusion Balloon Catheter
QXMedical, LLC
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