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SMARTWIRE PRESSURE GUIDE WIRE, MODEL 66XX

K070487 Class II Special
Decision Date
2007-03-16
Sponsor / Applicant
Volcano Corporation

Technical Specification

510(k) Submission ID K070487
Product Code DXO
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2870
Decision Date 2007-03-16
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SMARTWIRE PRESSURE GUIDE WIRE, MODEL 66XX received FDA 510(k) clearance under submission number K070487, sponsored by Volcano Corporation. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2007-03-16.

Classification & Regulation

This clearance is catalogued under FDA product code DXO and 21 CFR 870.2870, within the Cardiovascular review panel as a Class II device.