FDA 510(k) Applications Submitted by Prytime Medical Devices, Inc
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K170411 | 02/10/2017 | ER-REBOA Catheter | Prytime Medical Devices, Inc |
| K193440 | 12/11/2019 | ER-REBOA PLUS Catheter | Prytime Medical Devices, Inc |
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