FDA 510(k) Applications Submitted by Rob Yamashita

FDA 510(k) Number Submission Date Device Name Applicant
K122313 08/01/2012 STRYKER UNIVERSAL SMARTLOCK HYBRID MMF SYSTEM Stryker
K132519 08/12/2013 STRYKER CUSTOMIZED MANDIBLE RECON PLATE KIT Stryker
K112557 09/02/2011 STRYKER UNIVERSAL NEURO 3 SYSTEM Stryker
K093108 10/01/2009 STRYKER BIPOLAR FORCEPS Stryker Leibinger GmbH & Co. KG
K173373 10/27/2017 SafeT T-Piece Resuscitator Ventlab, LLC
K092743 09/08/2009 THE LEIBINGER ADVANCE INTERNAL MIDFACE DISTRACTION SYSTEM STRYKER CRANIOMAXILLOFACIAL
K233098 09/26/2023 MYOTouch Muscle Stimulator SunMed LLC.


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