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FDA 510(k) Applications Submitted by MEDIPLUS LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K013704
11/08/2001
MEDIPLUS SINGLE USE GI MANOMETRY CATHETER
MEDIPLUS LTD.
K031617
05/23/2003
MEDIPLUS SINGLE USE LOWER GI MANOMETRY CATHETER
MEDIPLUS LTD.
K131339
05/09/2013
CAPNOMASK
MEDIPLUS LTD.
K132890
09/16/2013
SUPRAPUBIC CATHETER AND INTRODUCER SET
MEDIPLUS LTD.
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