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FDA 510(k) Applications Submitted by CORTECHS LABS, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K032186
07/17/2003
AUTOALIGN
CORTECHS LABS, INC.
K012563
08/09/2001
DEEP GRAY
CORTECHS LABS, INC.
K021191
04/15/2002
AUTOALIGN
CORTECHS LABS, INC.
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