FDA 510(k) Applications Submitted by LUMIQUICK DIAGNOSTICS, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K130213 | 01/29/2013 | QUICKPROFILE SINGLE DRUG OF ABUSE DEVICE AND QUICK PROFILE MULTI-DRUGS OF ABUSE SCREEN DEVICE | LUMIQUICK DIAGNOSTICS, INC. |
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