meddevicedb.com FDA Device Reference

NC EMERGE PTCA DILATATION CATHETER (MONORAIL), NC EMERGE PTCA DILATATION CATHETER (OVER-THE-WIRE)

K141236 Class II Traditional
Decision Date
2014-08-07
Sponsor / Applicant
Boston Scientific Corporation

Technical Specification

510(k) Submission ID K141236
Product Code LOX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5100
Decision Date 2014-08-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NC EMERGE PTCA DILATATION CATHETER (MONORAIL), NC EMERGE PTCA DILATATION CATHETER (OVER-THE-WIRE) received FDA 510(k) clearance under submission number K141236, sponsored by Boston Scientific Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2014-08-07.

Classification & Regulation

This clearance is catalogued under FDA product code LOX and 21 CFR 870.5100, within the Cardiovascular review panel as a Class II device.