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CVIS INSIGHT IMAGING CATHETER

K924922 Class II Traditional
Decision Date
1993-06-29
Sponsor / Applicant
Cardiovascular Imaging Systems, Inc.

Technical Specification

510(k) Submission ID K924922
Product Code DQO
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1200
Decision Date 1993-06-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CVIS INSIGHT IMAGING CATHETER received FDA 510(k) clearance under submission number K924922, sponsored by Cardiovascular Imaging Systems, 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 1993-06-29.

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.