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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