FDA 510(k) Applications Submitted by CHROMOGENEX TECHNOLOGIES LTD
| 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 |
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