FDA 510(k) Applications Submitted by AcuVu Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K180096 | 01/16/2018 | GDT-1000 System | AcuVu Inc. |
| K211227 | 04/23/2021 | HTx Disposable Hysteroscope System | AcuVu Inc. |
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