meddevicedb.com FDA Device Reference

ONE Snare Endovascular Microsnare System

K142265 Class II Traditional
Decision Date
2014-11-13
Sponsor / Applicant
Merit Medical Systems, Inc.

Technical Specification

510(k) Submission ID K142265
Product Code MMX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5150
Decision Date 2014-11-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ONE Snare Endovascular Microsnare System received FDA 510(k) clearance under submission number K142265, sponsored by Merit Medical Systems, 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 2014-11-13.

Classification & Regulation

This clearance is catalogued under FDA product code MMX and 21 CFR 870.5150, within the Cardiovascular review panel as a Class II device.