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FDA 510(k) Applications Submitted by MATHEW PEXA
FDA 510(k) Number
Submission Date
Device Name
Applicant
K140482
02/26/2014
MANDREL GUIDEWIRE
LAKE REGION MEDICAL
K140485
02/26/2014
MANDREL GUIDEWIRE
LAKE REGION MEDICAL
K130798
03/22/2013
PRE-FORMED GUIDEWIRES
LAKE REGION MEDICAL, INC.
K111288
05/06/2011
ANCHORWIRE GUIDEWIRE
LAKE REGION MEDICAL
K151244
05/11/2015
Pre-Formed Guidewire
Lake Region Medical
K142393
08/27/2014
PREDICATE III GUIDEWIRE
LAKE REGION MEDICAL
K142397
08/27/2014
Predicate III Guidewire
Lake Region Medical
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