FDA 510(k) Applications Submitted by ACRO Biotech, Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K180771 | 03/23/2018 | Acro HCG Pregnancy Rapid Test | ACRO Biotech, Inc. |
| K172512 | 08/21/2017 | ACRO HCG Pregnancy Rapid Test | ACRO Biotech, Inc. |
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