FDA 510(k) Applications Submitted by GTIMD LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K202427 | 08/25/2020 | Aqueduct 100 Plus Cervical Dilation Balloon Catheter | GTIMD LLC |
| K202433 | 08/25/2020 | Aqueduct 200 Cervical Dilation Balloon Catheter | GTIMD LLC |
| K160664 | 03/09/2016 | Aqueduct 100 Cervical Dilator | GTIMD LLC |
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