FDA 510(k) Applications Submitted by neoSurgical Ltd

FDA 510(k) Number Submission Date Device Name Applicant
K142903 10/06/2014 neoClose 2 AutoAnchor Pack US, neoClose 4 AutoAnchor Pack US NEOSURGICAL LTD
K131688 06/10/2013 NEOCLOSE HASSON, NEOCLOSE UNIVERSAL NEOSURGICAL LTD
K123280 10/22/2012 NEOCLOSE HASSON, NEOCLOSE UNIVERSAL NEOSURGICAL LTD
K173917 12/22/2017 neoClose PDS neoSurgical Ltd


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