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FDA 510(k) Applications Submitted by Boddingtons Plastics Ltd
FDA 510(k) Number
Submission Date
Device Name
Applicant
K122565
08/22/2012
ARC ENDOCUFF
BODDINGTONS PLASTICS LTD
K151801
07/02/2015
Arc Endocuff Vision
BODDINGTONS PLASTICS LTD
K162205
08/05/2016
Arc EndoCuff and Arc EndoCuff Vision
BODDINGTONS PLASTICS LTD
K191067
04/22/2019
Arc Endocuff Glide AEG110 & AEG120
Boddingtons Plastics Ltd
K191330
05/16/2019
Arc Enterocuff
Boddingtons Plastics Ltd
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