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FDA 510(k) Applications Submitted by ENVISIONEERING, LLC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K073399
12/04/2007
TARGETSCAN BIOPSY KIT, TARGETSCAN BIOPSY NEEDLE GUIDE
ENVISIONEERING, LLC.
K041637
06/17/2004
TARGETSCAN TRANSRECTAL ULTRASOUND SYSTEM
ENVISIONEERING, LLC.
K041638
06/17/2004
TARGETSCAN BIOPSY KIT
ENVISIONEERING, LLC.
K041639
06/17/2004
TARGETSCN TRANSRECTAL ULTRASOUND SYSTEM
ENVISIONEERING, LLC.
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