FDA 510(k) Applications Submitted by PETER R BEVAN

FDA 510(k) Number Submission Date Device Name Applicant
K101366 05/17/2010 I-LIPO, MODELS A00-1238 (230V), A00-1239 (120V) CHROMOGENEX TECHNOLOGIES LTD
K111501 05/31/2011 I-LIPO SYSTEM CHROMOGENEX TECHNOLOGIES LIMITED
K081619 06/09/2008 CHROMOLITE EP CHROMOGENEX TECHNOLOGIES LIMITED


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