FDA 510(k) Applications Submitted by DEBORA DEMERS, PH.D.

FDA 510(k) Number Submission Date Device Name Applicant
K121571 05/29/2012 TUBECLEAR ACTUATED MEDICAL, INC
K131052 04/15/2013 TUBECLEAR MODEL 101 (WITH NEW CLEARING STEM NE AND G MODELS) ACTUATED MEDICAL, INC.
K123659 11/28/2012 TUBE-CLEAR, CONTROL BOX (COMPONENT OF TUBECLEAR), CLEARING STEM (COMPONENT OF TUBECLEAR) ACTUATED MEDICAL, INC.


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