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FDA 510(k) Applications Submitted by ACCUTECH MEDICAL TECHNOLOGIES, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K090281
02/05/2009
ACCUTECH FAMILY OF POWERFLEX LASER DELIVERY DEVICES
ACCUTECH MEDICAL TECHNOLOGIES, INC.
K061025
04/13/2006
ACCUTECH ENDOLITE PROBE
ACCUTECH MEDICAL TECHNOLOGIES, INC.
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