FDA 510(k) Applications for Medical Device Product Code "PTE"
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K170120 | Interscope, Inc | EndoRotor | 04/18/2017 |
| K181127 | Interscope, Inc. | EndoRotor Console, EndoRotor Catheters, EndoRotor Specimen Trap, EndoRotor Filter Set, EndoRotor Foot Control | 01/03/2019 |
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