FDA 510(k) Applications Submitted by JASON SKRAMSTED

FDA 510(k) Number Submission Date Device Name Applicant
K120040 01/05/2012 REPROCESSED SURGICAL ELECTRIC INSTRUMENT STERILMED, INC.
K120204 01/23/2012 REPROCESSED FEMORAL COMPRESSION DEVICE STERILMED, INC.
K121158 04/16/2012 REPROCESSED ELECTROPHYSIOLOGY DIAGNOSTIC CATHETERS STERILMED, INC.
K123096 10/02/2012 REPROCESSED VESSEL SEALER STERILMED, INC.
K133414 11/07/2013 REPROCESSED CLOSURE SYSTEM STERILMED, INC.
K121240 04/24/2012 REPROCESSED ENDOSCOPIC TROCARS STERILMED, INC.


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