FDA 510(k) Applications Submitted by Interscope, Inc.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K190715 |
03/19/2019 |
EndoRotor Console, EndoRotor Catheter, EndoRotor Specimen Trap, EndoRotor Filter Set, EndoRotor Roll Stand |
Interscope, Inc. |
K181127 |
04/30/2018 |
EndoRotor Console, EndoRotor Catheters, EndoRotor Specimen Trap, EndoRotor Filter Set, EndoRotor Foot Control |
Interscope, Inc. |
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