FDA 510(k) Applications Submitted by QSERVE AMERICA, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K123514 | 11/14/2012 | CLEARPATH ALIGNER | QSERVE AMERICA, INC. |
| K110246 | 01/27/2011 | MEDISIZE RED AND MEDISIZE BLUE | QSERVE AMERICA, INC. |
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