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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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