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CATHETER SYSTEM, COPE/EISENBERG

K772175 Class II Traditional
Decision Date
1977-11-28
Sponsor / Applicant
Victory Engineering Corp.

Technical Specification

510(k) Submission ID K772175
Product Code DQO
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1200
Decision Date 1977-11-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CATHETER SYSTEM, COPE/EISENBERG received FDA 510(k) clearance under submission number K772175, sponsored by Victory Engineering 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 1977-11-28.

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.