meddevicedb.com FDA Device Reference

SHORT INTRODUCER SHEATH

K032569 Class II Special
Decision Date
2003-09-16
Sponsor / Applicant
Rex Medical

Technical Specification

510(k) Submission ID K032569
Product Code DYB
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1340
Decision Date 2003-09-16
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SHORT INTRODUCER SHEATH received FDA 510(k) clearance under submission number K032569, sponsored by Rex Medical. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2003-09-16.

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.