FDA 510(k) Applications Submitted by Interscope, Inc
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| DEN200016 | 03/16/2020 | EndoRotor Device | Interscope, Inc |
| K170120 | 01/13/2017 | EndoRotor | Interscope, Inc |
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