meddevicedb.com FDA Device Reference

BENZALKONIUM-HEPARIN COATED GUIDEWIRES

K802473 Class II Traditional
Decision Date
1980-11-12
Sponsor / Applicant
Medrad, Inc.

Technical Specification

510(k) Submission ID K802473
Product Code DQX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1330
Decision Date 1980-11-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BENZALKONIUM-HEPARIN COATED GUIDEWIRES received FDA 510(k) clearance under submission number K802473, sponsored by Medrad, 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 1980-11-12.

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.