FDA 510(k) Applications Submitted by BTL INDUSTRIES LTD

FDA 510(k) Number Submission Date Device Name Applicant
K134040 12/31/2013 BTL-9000; BTL-9000 RADIOFREQUENCY MODULE BTL INDUSTRIES LTD
K092191 07/21/2009 EXILIS, MODEL 5000 BTL INDUSTRIES LTD
K122966 09/25/2012 XP200 BTL INDUSTRIES LTD


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