FDA 510(k) Applications Submitted by ABMRC LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K191912 | 07/17/2019 | BiWaze Cough | ABMRC LLC |
| K213564 | 11/09/2021 | BiWaze Clear System | ABMRC LLC |
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