Clearance Summary
Medline ReNewal Reprocessed Biosense Webster Webster CS Catheter with EZ Steer Technology and Medline ReNewal Reprocessed Biosense Webster Webster CS Catheter with EZ Steer Technology and Auto ID Technology (BD710DF282CT, BD710DF282RTS, BD710FJ282RTS, BD710FJ282CT) received FDA 510(k) clearance under submission number K241224, sponsored by Surgical Instrument Service and Savings Inc.(Dba Medline Ren. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2024-11-15.
- Submission: K241224
- Applicant / Sponsor: Surgical Instrument Service and Savings Inc.(Dba Medline Ren
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1220
- Decision date: 2024-11-15
Classification & Regulation
This clearance is catalogued under FDA product code NLH and 21 CFR 870.1220, within the Cardiovascular review panel as a Class II device.