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FDA 510(k) Applications Submitted by GYNETECH PTY. LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K150519
03/02/2015
ManipulatOR PRO, ManipulatOR
GYNETECH PTY. LTD.
K051594
06/16/2005
MCCARTNEY ACCESS TUBE
GYNETECH PTY. LTD.
K142164
08/06/2014
MANIPULATOR; MANIPULATOR PRO
GYNETECH PTY. LTD.
K142700
09/22/2014
InsufflatOR Needle
GYNETECH PTY. LTD.
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