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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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