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Visions PV .035 Digital IVUS Catheter

K153094 Class II Special
Decision Date
2015-12-31
Sponsor / Applicant
Volcano Corporation

Technical Specification

510(k) Submission ID K153094
Product Code OBJ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1200
Decision Date 2015-12-31
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Visions PV .035 Digital IVUS Catheter received FDA 510(k) clearance under submission number K153094, 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 2015-12-31.

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.