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BOSTON SCIENTIFIC SCIMED ATLANTIS CORONARY IMAGING CATHETER, MODEL C4020

K000743 Class II Traditional
Decision Date
2000-09-06
Sponsor / Applicant
Boston Scientific Scimed, Inc.

Technical Specification

510(k) Submission ID K000743
Product Code DQO
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1200
Decision Date 2000-09-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BOSTON SCIENTIFIC SCIMED ATLANTIS CORONARY IMAGING CATHETER, MODEL C4020 received FDA 510(k) clearance under submission number K000743, sponsored by Boston Scientific Scimed, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2000-09-06.

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.