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PROGRAMMER MODEL 2035/ELECTROGRAM CABLE MODEL 6580

K863045 Class III Traditional
Decision Date
1986-09-29
Sponsor / Applicant
Cardiac Pacemakers, Inc.

Technical Specification

510(k) Submission ID K863045
Product Code KRG
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3700
Decision Date 1986-09-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PROGRAMMER MODEL 2035/ELECTROGRAM CABLE MODEL 6580 received FDA 510(k) clearance under submission number K863045, sponsored by Cardiac Pacemakers, 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 1986-09-29.

Classification & Regulation

This clearance is catalogued under FDA product code KRG and 21 CFR 870.3700, within the Cardiovascular review panel as a Class III device.