Clearance Summary
SINGLE NEEDLE SUBCLAVIAN VEIN MWI250/260 received FDA 510(k) clearance under submission number K831440, sponsored by Med-West, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1983-06-03.
- Submission: K831440
- Applicant / Sponsor: Med-West, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5540
- Decision date: 1983-06-03
Classification & Regulation
This clearance is catalogued under FDA product code FIQ and 21 CFR 876.5540, within the Gastroenterology, Urology review panel as a Class II device.