Clearance Summary
VACUCATH I.V. CATHETER INTRODUCTER received FDA 510(k) clearance under submission number K003187, sponsored by Auto/Cath Vascular Access, Inc.. 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 2001-05-21.
- Submission: K003187
- Applicant / Sponsor: Auto/Cath Vascular Access, Inc.
- Clearance pathway: Traditional
- Review panel: General Hospital
- Device class: Class II
- Regulation citation: 21 CFR 880.5200
- Decision date: 2001-05-21
Classification & Regulation
This clearance is catalogued under FDA product code FOZ and 21 CFR 880.5200, within the General Hospital review panel as a Class II device.