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FDA 510(k) Applications Submitted by Andrew Jones
FDA 510(k) Number
Submission Date
Device Name
Applicant
K100267
01/29/2010
FLEXIMARC, MODEL CM-0.9-2-10-GG-L
CORTEX MANUFACTURING, INC.
K142294
08/18/2014
FlexiMarc Marker
CORTEX MANUFACTURING, INC.
K102506
09/01/2010
MIXED MEDIA MARKER
CORTEX MANUFACTURING, INC.
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