FDA 510(k) Applications Submitted by QUICKLASE LIMITED
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K100474 | 02/18/2010 | QUICKLASEDUAL+, QUICKLASE810, QUICKLASE810, QUICKLASE980, QUICKLASE980 MODEL: 3W,5W,3W,5W | QUICKLASE LIMITED |
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