FDA 510(k) Applications Submitted by AMERITEK USA, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K061257 | 05/04/2006 | DBEST HCG PANEL TEST KIT | AMERITEK USA, INC. |
| K071242 | 05/03/2007 | DBEST ONE STEP OCCULT BLOOD TEST KITS | AMERITEK USA, INC. |
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