FDA 510(k) Applications Submitted by CHROMOGENEX TECHNOLOGIES LIMITED
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K111501 | 05/31/2011 | I-LIPO SYSTEM | CHROMOGENEX TECHNOLOGIES LIMITED |
| K081619 | 06/09/2008 | CHROMOLITE EP | CHROMOGENEX TECHNOLOGIES LIMITED |
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