meddevicedb.com FDA Device Reference

Crossing Support Catheter

K183305 Class II Traditional
Decision Date
2019-08-05
Sponsor / Applicant
Tractus Vascular, LLC

Technical Specification

510(k) Submission ID K183305
Product Code DQY
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1250
Decision Date 2019-08-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Crossing Support Catheter received FDA 510(k) clearance under submission number K183305, sponsored by Tractus Vascular, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2019-08-05.

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.