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MODIFICATIONS TO ACS CORONARY GUIDING CATHETER W/T

K851574 Class II Traditional
Decision Date
1985-06-19
Sponsor / Applicant
Advanced Cardiovascular Systems, Inc.

Technical Specification

510(k) Submission ID K851574
Product Code DQX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1330
Decision Date 1985-06-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODIFICATIONS TO ACS CORONARY GUIDING CATHETER W/T received FDA 510(k) clearance under submission number K851574, sponsored by Advanced Cardiovascular 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 1985-06-19.

Classification & Regulation

This clearance is catalogued under FDA product code DQX and 21 CFR 870.1330, within the Cardiovascular review panel as a Class II device.