Clearance Summary
LIFE-LINE(TM) VASCULAR ACCESS SYSTEM received FDA 510(k) clearance under submission number K895030, sponsored by Medical Engineering and Development Institute. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1990-04-17.
- Submission: K895030
- Applicant / Sponsor: Medical Engineering and Development Institute
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5965
- Decision date: 1990-04-17
Classification & Regulation
This clearance is catalogued under FDA product code LJT and 21 CFR 880.5965, within the General Hospital review panel as a Class II device.