Clearance Summary
MULTI-LUMEN INTRAVENOUS INFUSION CATH received FDA 510(k) clearance under submission number K833825, sponsored by Medical Parameters, 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 1984-01-10.
- Submission: K833825
- Applicant / Sponsor: Medical Parameters, Inc.
- Clearance pathway: Traditional
- Review panel: Cardiovascular
- Device class: Class II
- Regulation citation: 21 CFR 870.1250
- Decision date: 1984-01-10
Classification & Regulation
This clearance is catalogued under FDA product code DQY and 21 CFR 870.1250, within the Cardiovascular review panel as a Class II device.