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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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