Clearance Summary
Medline ReNewal Reprocessed Abbott Inquiry Steerable Diagnostic Catheter received FDA 510(k) clearance under submission number K242225, sponsored by Surgical Instrument Service and Savings, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2024-11-29.
- Submission: K242225
- Applicant / Sponsor: Surgical Instrument Service and Savings, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1220
- Decision date: 2024-11-29
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.