meddevicedb.com FDA Device Reference

MODEL 340 SERIES UNIPOLAR & MODEL 5000B PROGRAMMER

K905403 Class III Traditional
Decision Date
1991-10-16
Sponsor / Applicant
Cook Pacemaker Corp.

Technical Specification

510(k) Submission ID K905403
Product Code DXY
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3610
Decision Date 1991-10-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL 340 SERIES UNIPOLAR & MODEL 5000B PROGRAMMER received FDA 510(k) clearance under submission number K905403, sponsored by Cook Pacemaker 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 1991-10-16.

Classification & Regulation

This clearance is catalogued under FDA product code DXY and 21 CFR 870.3610, within the Cardiovascular review panel as a Class III device.