FDA 510(k) Applications Submitted by Dan Rottenberg
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K211802 | 06/10/2021 | GoBack Crossing Catheter | Upstream Peripheral Technologies, Ltd |
| K182937 | 10/22/2018 | Upstream GoBack Crossing Catheter | Upstream Peripheral Technologies, Ltd. |
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