Clearance Summary
ATLANTIS PV IMAGING CATHETER, MODEL 36456 received FDA 510(k) clearance under submission number K022860, sponsored by Boston Scientific, Target. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2002-11-21.
- Submission: K022860
- Applicant / Sponsor: Boston Scientific, Target
- Clearance pathway: Special
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1570
- Decision date: 2002-11-21
Classification & Regulation
This clearance is catalogued under FDA product code ITX and 21 CFR 892.1570, within the Radiology review panel as a Class II device.