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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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