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FDA 510(k) Applications Submitted by TOM NOLAN
FDA 510(k) Number
Submission Date
Device Name
Applicant
K120585
02/27/2012
CONVEY GUIDING CATHETER
PENDRACARE INTERNATIONAL, B.V.
K132197
07/16/2013
CONVEY 7F GUIDING CATHETER, CONVEY 8F GUIDING CATHETER
PENDRACARE INTERNATIONAL, B.V.
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