meddevicedb.com FDA Device Reference

EVOLUTION RL CONTROLLED-ROTATION DILATOR SHEATH SET, EVOLUTION SHORTIE RL CONTROLLED-ROTATION DILATOR SHEATH SET

K141148 Class II Traditional
Decision Date
2014-07-01
Sponsor / Applicant
Cook Vascular, Inc.

Technical Specification

510(k) Submission ID K141148
Product Code DRE
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1310
Decision Date 2014-07-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EVOLUTION RL CONTROLLED-ROTATION DILATOR SHEATH SET, EVOLUTION SHORTIE RL CONTROLLED-ROTATION DILATOR SHEATH SET received FDA 510(k) clearance under submission number K141148, sponsored by Cook Vascular, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2014-07-01.

Classification & Regulation

This clearance is catalogued under FDA product code DRE and 21 CFR 870.1310, within the Cardiovascular review panel as a Class II device.