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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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