FDA 510(k) Applications Submitted by HEMEDEX INCORPORATED

FDA 510(k) Number Submission Date Device Name Applicant
K141869 07/11/2014 QFLOW 500 TITANIUM BOLT, QUAD LUMEN BOLT KIT HEMEDEX INCORPORATED
K032127 07/10/2003 HEMEDEX FIXATION DEVICE HEMEDEX INCORPORATED
K032337 07/29/2003 HEMEDEX CRANIAL BOLT MODELS, 3601, 3602 HEMEDEX INCORPORATED
K013376 10/11/2001 QFLOW 500 PERFUSION MONITORING SYSTEM HEMEDEX INCORPORATED


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