FDA 510(k) Applications Submitted by Acon Laboratories Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K193318 | 12/02/2019 | Distinct« Early Detection Pregnancy Test | Acon Laboratories Inc. |
| K163406 | 12/05/2016 | Mission Cholesterol Monitoring System, Mission Cholesterol Pro Monitoring System | ACON LABORATORIES INC. |
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