FDA 510(k) Applications Submitted by INVUITY, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K090070 01/12/2009 INVUITY BRITEFIELD MCCULLOCH RETRACTOR SYSTEM INVUITY, INC.
K113697 12/16/2011 EIGR SURGICAL ILLUMINATION SYSTEM INVUITY, INC.


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