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ITC COAXIAL ANGIOGRAPHIC CATH SET, MODIFICATION

K912477 Class II Traditional
Decision Date
1991-11-05
Sponsor / Applicant
Interventional Therapeutics Corp.

Technical Specification

510(k) Submission ID K912477
Product Code DQO
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1200
Decision Date 1991-11-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ITC COAXIAL ANGIOGRAPHIC CATH SET, MODIFICATION received FDA 510(k) clearance under submission number K912477, sponsored by Interventional Therapeutics Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1991-11-05.

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.