FDA 510(k) Applications Submitted by DAN FULLERTON
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K141410 | 05/29/2014 | ORAGENE DX OGD-500.001 | DNA GENOTEK, INC. |
| K152464 | 08/31/2015 | ORAcollect.Dx | DNA GENOTEK INC. |
| K152556 | 09/08/2015 | Oragene Dx | DNA Genotek Inc |
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