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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