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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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