Clearance Summary
VAS-CATH CATHETER REPAIR KIT received FDA 510(k) clearance under submission number K883768, sponsored by Vas-Cath, 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 1988-11-14.
- Submission: K883768
- Applicant / Sponsor: Vas-Cath, Inc.
- Clearance pathway: Traditional
- Review panel: Gastroenterology, Urology
- Device class: Class II
- Regulation citation: 21 CFR 876.5540
- Decision date: 1988-11-14
Classification & Regulation
This clearance is catalogued under FDA product code LFJ and 21 CFR 876.5540, within the Gastroenterology, Urology review panel as a Class II device.