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VISIONS PV .035 DITITAL IVUS CATHETER

K121273 Class II Abbreviated
Decision Date
2012-09-10
Sponsor / Applicant
Volcano Corporation

Technical Specification

510(k) Submission ID K121273
Product Code OBJ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1200
Decision Date 2012-09-10
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VISIONS PV .035 DITITAL IVUS CATHETER received FDA 510(k) clearance under submission number K121273, sponsored by Volcano Corporation. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2012-09-10.

Classification & Regulation

This clearance is catalogued under FDA product code OBJ and 21 CFR 870.1200, within the Cardiovascular review panel as a Class II device.