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DIALOG PROGRAMMER 700 - PROGRAM VERSION 6.37

K860546 Class III Traditional
Decision Date
1986-04-23
Sponsor / Applicant
Pacesetter Systems

Technical Specification

510(k) Submission ID K860546
Product Code KRG
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3700
Decision Date 1986-04-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DIALOG PROGRAMMER 700 - PROGRAM VERSION 6.37 received FDA 510(k) clearance under submission number K860546, sponsored by Pacesetter Systems. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1986-04-23.

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.