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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