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EASYTRAK 2 STYLET, MODELS 4826, 4829, 4832.

K052965 Class II Traditional
Decision Date
2006-02-13
Sponsor / Applicant
Guidant Corporation

Technical Specification

510(k) Submission ID K052965
Product Code DRB
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1380
Decision Date 2006-02-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EASYTRAK 2 STYLET, MODELS 4826, 4829, 4832. received FDA 510(k) clearance under submission number K052965, sponsored by Guidant 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 2006-02-13.

Classification & Regulation

This clearance is catalogued under FDA product code DRB and 21 CFR 870.1380, within the Cardiovascular review panel as a Class II device.