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IMAGER II ANGIOGRAPHIC CATHETERS

K120893 Class II Special
Decision Date
2012-03-29
Sponsor / Applicant
Boston Scientific Corp

Technical Specification

510(k) Submission ID K120893
Product Code DQO
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1200
Decision Date 2012-03-29
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IMAGER II ANGIOGRAPHIC CATHETERS received FDA 510(k) clearance under submission number K120893, sponsored by Boston Scientific Corp. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2012-03-29.

Classification & Regulation

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