FDA 510(k) Applications Submitted by Actuated Medical, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
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.
K200646 03/12/2020 TubeClear System Actuated Medical, Inc.
K172556 08/24/2017 TubeClear System Actuated Medical, Inc.
K163092 11/04/2016 TubeClear Control Box and Clearing Stem Actuated Medical, Inc.


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