Clearance Summary
EndoRotor Console, EndoRotor Catheters, EndoRotor Specimen Trap, EndoRotor Filter Set, EndoRotor Foot Control received FDA 510(k) clearance under submission number K181127, sponsored by Interscope, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 2019-01-03.
- Submission: K181127
- Applicant / Sponsor: Interscope, Inc.
- Clearance pathway: Traditional
- Review panel: Obstetrics/Gynecology
- Device class: Class II
- Regulation citation: 21 CFR 884.1690
- Decision date: 2019-01-03
Classification & Regulation
This clearance is catalogued under FDA product code PTE and 21 CFR 884.1690, within the Obstetrics/Gynecology review panel as a Class II device.