meddevicedb.com FDA Device Reference

SENTRANT INTRODUCER SHEATH WITH HYDROPHILIC COATING

K123990 Class II Traditional
Decision Date
2013-04-26
Sponsor / Applicant
Medtronic Vascular

Technical Specification

510(k) Submission ID K123990
Product Code DYB
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1340
Decision Date 2013-04-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SENTRANT INTRODUCER SHEATH WITH HYDROPHILIC COATING received FDA 510(k) clearance under submission number K123990, sponsored by Medtronic Vascular. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2013-04-26.

Classification & Regulation

This clearance is catalogued under FDA product code DYB and 21 CFR 870.1340, within the Cardiovascular review panel as a Class II device.